Canonical Allele Identifier: CA14383547
Gene: STRADA HGNC NCBI

Linked Data

dbSNP Id: rs721575

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63705560C>T , CM000679.2:g.63705560C>T GRCh38
NC_000017.10:g.61782920C>T , CM000679.1:g.61782920C>T GRCh37
NC_000017.9:g.59136652C>T NCBI36
NG_015817.1:g.41411G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000245865.10:c.676-652G>A ENSP00000245865.5:n.676-652G>A
ENST00000336174.12:c.859-978G>A MANE Select ENSP00000336655.6:n.859-978G>A
ENST00000375840.9:c.685-978G>A ENSP00000365000.4:n.685-978G>A
ENST00000392950.9:c.748-978G>A ENSP00000376677.4:n.748-978G>A
ENST00000447001.8:c.727-978G>A ENSP00000398841.3:n.727-978G>A
ENST00000578008.6:c.772-652G>A ENSP00000464547.2:n.772-652G>A
ENST00000578801.6:c.687-652G>A ENSP00000463872.2:n.687-652G>A
ENST00000579318.2:n.1182-978G>A
ENST00000580039.6:c.662-978G>A
ENST00000582137.6:c.772-978G>A ENSP00000462922.1:n.772-978G>A
ENST00000638193.1:c.859-978G>A ENSP00000491928.1:n.859-978G>A
ENST00000638276.1:c.685-978G>A ENSP00000491922.1:n.685-978G>A
ENST00000638309.1:c.859-652G>A ENSP00000492877.1:n.859-652G>A
ENST00000638698.1:c.858+1075G>A ENSP00000491082.1:n.858+1075G>A
ENST00000638702.1:c.685-978G>A ENSP00000491017.1:n.685-978G>A
ENST00000638708.1:c.772-978G>A ENSP00000491580.1:n.772-978G>A
ENST00000638888.1:c.859-978G>A ENSP00000491528.1:n.859-978G>A
ENST00000639135.1:c.739-978G>A ENSP00000491843.1:n.739-978G>A
ENST00000639521.1:c.576-978G>A ENSP00000492087.1:n.576-978G>A
ENST00000639835.1:c.748-978G>A ENSP00000492578.1:n.748-978G>A
ENST00000640086.1:c.748-978G>A ENSP00000492238.1:n.748-978G>A
ENST00000640174.1:c.835-978G>A ENSP00000491380.1:n.835-978G>A
ENST00000640183.1:n.2280-978G>A
ENST00000640397.1:c.686+1075G>A ENSP00000492379.1:n.686+1075G>A
ENST00000640679.1:c.858+1075G>A ENSP00000491092.1:n.858+1075G>A
ENST00000640827.1:c.687-978G>A ENSP00000492499.1:n.687-978G>A
ENST00000640870.1:c.582-978G>A ENSP00000492479.1:n.582-978G>A
ENST00000640979.1:c.685-978G>A ENSP00000491485.1:n.685-978G>A
ENST00000640999.1:c.748-978G>A ENSP00000491643.1:n.748-978G>A
ENST00000245865.9:c.676-652G>A ENSP00000245865.5:n.676-652G>A
ENST00000336174.10:c.859-978G>A ENSP00000336655.6:n.859-978G>A
ENST00000375840.8:c.685-978G>A ENSP00000365000.4:n.685-978G>A
ENST00000392950.8:c.748-978G>A ENSP00000376677.4:n.748-978G>A
ENST00000447001.7:c.727-978G>A ENSP00000398841.3:n.727-978G>A
ENST00000578008.5:c.475-652G>A ENSP00000464547.1:n.475-652G>A
ENST00000578801.5:c.378-652G>A ENSP00000463872.1:n.378-652G>A
ENST00000579340.5:c.513-978G>A ENSP00000462530.1:n.513-978G>A
ENST00000580039.5:n.710-978G>A
ENST00000580553.1:c.937-978G>A
ENST00000582137.5:c.772-978G>A ENSP00000462922.1:n.772-978G>A
ENST00000583085.1:n.965G>A
ENST00000617949.4:c.676-652G>A ENSP00000481505.1:n.676-652G>A
NM_001003786.2:c.748-978G>A NP_001003786.1:n.748-978G>A
NM_001003787.2:c.859-978G>A NP_001003787.1:n.859-978G>A
NM_001003788.2:c.685-978G>A NP_001003788.1:n.685-978G>A
NM_001165969.1:c.772-978G>A NP_001159441.1:n.772-978G>A
NM_001165970.1:c.727-978G>A NP_001159442.1:n.727-978G>A
NM_153335.5:c.748-978G>A NP_699166.2:n.748-978G>A
XM_005257797.1:c.835-978G>A XP_005257854.1:n.835-978G>A
XM_005257798.1:c.772-978G>A XP_005257855.1:n.772-978G>A
XM_005257799.1:c.685-978G>A XP_005257856.1:n.685-978G>A
XM_005257800.1:c.859-978G>A XP_005257857.1:n.859-978G>A
XM_005257801.3:c.859-652G>A XP_005257858.1:n.859-652G>A
XM_005257803.3:c.687-652G>A XP_005257860.1:n.687-652G>A
XM_011525466.1:c.859-978G>A XP_011523768.1:n.859-978G>A
XM_011525467.1:c.754-978G>A XP_011523769.1:n.754-978G>A
XR_243687.1:n.836-978G>A
XR_243688.1:n.836-978G>A
NM_001003786.3:c.748-978G>A NP_001003786.1:n.748-978G>A
NM_001003787.3:c.859-978G>A NP_001003787.1:n.859-978G>A
NM_001003788.3:c.685-978G>A NP_001003788.1:n.685-978G>A
NM_001165969.2:c.772-978G>A NP_001159441.1:n.772-978G>A
NM_001165970.2:c.727-978G>A NP_001159442.1:n.727-978G>A
NM_001363786.1:c.835-978G>A NP_001350715.1:n.835-978G>A
NM_001363787.1:c.772-978G>A NP_001350716.1:n.772-978G>A
NM_001363788.1:c.859-978G>A NP_001350717.1:n.859-978G>A
NM_001363789.1:c.748-978G>A NP_001350718.1:n.748-978G>A
NM_001363790.1:c.685-978G>A NP_001350719.1:n.685-978G>A
NM_001363791.1:c.685-978G>A NP_001350720.1:n.685-978G>A
NM_153335.6:c.748-978G>A NP_699166.2:n.748-978G>A
NR_156741.1:n.977-978G>A
XM_005257799.3:c.685-978G>A XP_005257856.1:n.685-978G>A
XM_005257801.5:c.859-652G>A XP_005257858.1:n.859-652G>A
XM_005257803.5:c.687-652G>A XP_005257860.1:n.687-652G>A
XM_011525466.3:c.859-978G>A XP_011523768.1:n.859-978G>A
XM_011525467.3:c.754-978G>A XP_011523769.1:n.754-978G>A
XM_017025314.2:c.772-652G>A XP_016880803.1:n.772-652G>A
XR_243688.3:n.834-978G>A
NM_001003787.4:c.859-978G>A MANE Select NP_001003787.1:n.859-978G>A
NR_156741.2:n.790-978G>A