Canonical Allele Identifier: CA4851440
Gene: TRPS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2939276
ClinVar RCV Id: RCV003792002
dbSNP Id: rs778331175

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.115414075C>G , CM000670.2:g.115414075C>G GRCh38
NC_000008.10:g.116426303C>G , CM000670.1:g.116426303C>G GRCh37
NC_000008.9:g.116495479C>G NCBI36
NG_012383.3:g.259927G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395715.8:c.3833G>C MANE Select ENSP00000379065.3:p.Gly1278Ala
ENST00000640765.1:c.3794G>C ENSP00000492037.1:p.Gly1265Ala
ENST00000220888.9:c.3794G>C ENSP00000220888.5:p.Gly1265Ala
ENST00000395715.7:c.3833G>C ENSP00000379065.3:p.Gly1278Ala
ENST00000519076.5:c.3056G>C ENSP00000428910.1:p.Gly1019Ala
ENST00000520276.5:c.3806G>C ENSP00000428680.1:p.Gly1269Ala
NM_001282902.2:c.3806G>C NP_001269831.1:p.Gly1269Ala
NM_001282903.2:c.3812G>C NP_001269832.1:p.Gly1271Ala
NM_014112.4:c.3833G>C NP_054831.2:p.Gly1278Ala
XM_005251049.2:c.3794G>C XP_005251106.1:p.Gly1265Ala
XM_006716625.1:c.3833G>C XP_006716688.1:p.Gly1278Ala
XM_011517264.1:c.3833G>C XP_011515566.1:p.Gly1278Ala
XM_011517265.1:c.3833G>C XP_011515567.1:p.Gly1278Ala
XM_011517266.1:c.3833G>C XP_011515568.1:p.Gly1278Ala
XM_011517267.1:c.3812G>C XP_011515569.1:p.Gly1271Ala
XM_011517268.1:c.3794G>C XP_011515570.1:p.Gly1265Ala
NM_001330599.1:c.3794G>C NP_001317528.1:p.Gly1265Ala
XM_011517264.2:c.3833G>C XP_011515566.1:p.Gly1278Ala
XM_011517266.3:c.3833G>C XP_011515568.1:p.Gly1278Ala
XM_011517268.2:c.3794G>C XP_011515570.1:p.Gly1265Ala
NM_001282902.3:c.3806G>C NP_001269831.1:p.Gly1269Ala
NM_001282903.3:c.3812G>C NP_001269832.1:p.Gly1271Ala
NM_001330599.2:c.3794G>C NP_001317528.1:p.Gly1265Ala
NM_014112.5:c.3833G>C MANE Select NP_054831.2:p.Gly1278Ala