Canonical Allele Identifier: CA393128415
Gene: STRA6 HGNC NCBI

Linked Data

dbSNP Id: rs144308388

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74180193C>A , CM000677.2:g.74180193C>A GRCh38
NC_000015.9:g.74472534C>A , CM000677.1:g.74472534C>A GRCh37
NC_000015.8:g.72259587C>A NCBI36
NG_009207.1:g.33838G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395105.9:c.1891G>T MANE Select ENSP00000378537.4:p.Gly631Trp
ENST00000323940.9:c.1891G>T ENSP00000326085.5:p.Gly631Trp
ENST00000395105.8:c.1891G>T ENSP00000378537.4:p.Gly631Trp
ENST00000416286.7:c.1867G>T ENSP00000400403.3:p.Gly623Trp
ENST00000423167.6:c.1864G>T ENSP00000413012.2:p.Gly622Trp
ENST00000449139.6:c.1891G>T ENSP00000410221.2:p.Gly631Trp
ENST00000535552.5:c.2002G>T ENSP00000440238.1:p.Gly668Trp
ENST00000545137.5:n.1600G>T
ENST00000563965.5:c.2008G>T ENSP00000456609.1:p.Gly670Trp
ENST00000572785.1:c.746G>T
ENST00000574278.5:c.1936G>T ENSP00000458827.1:p.Gly646Trp
ENST00000574439.5:n.2163G>T
ENST00000616000.4:c.1891G>T ENSP00000479112.1:p.Gly631Trp
NM_001142617.1:c.1891G>T NP_001136089.1:p.Gly631Trp
NM_001142618.1:c.1891G>T NP_001136090.1:p.Gly631Trp
NM_001142619.1:c.1864G>T NP_001136091.1:p.Gly622Trp
NM_001199040.1:c.2002G>T NP_001185969.1:p.Gly668Trp
NM_001199041.1:c.1936G>T NP_001185970.1:p.Gly646Trp
NM_001199042.1:c.2008G>T NP_001185971.1:p.Gly670Trp
NM_022369.3:c.1891G>T NP_071764.3:p.Gly631Trp
XM_011521883.1:c.1891G>T XP_011520185.1:p.Gly631Trp
XM_011521884.1:c.1702G>T XP_011520186.1:p.Gly568Trp
XM_017022478.1:c.1939G>T XP_016877967.1:p.Gly647Trp
XM_017022479.1:c.1891G>T XP_016877968.1:p.Gly631Trp
XM_017022480.1:c.1702G>T XP_016877969.1:p.Gly568Trp
NM_022369.4:c.1891G>T MANE Select NP_071764.3:p.Gly631Trp
NM_001142617.2:c.1891G>T NP_001136089.1:p.Gly631Trp
NM_001142619.2:c.1864G>T NP_001136091.1:p.Gly622Trp
NM_001199042.2:c.2008G>T NP_001185971.1:p.Gly670Trp
NM_001142618.2:c.1891G>T NP_001136090.1:p.Gly631Trp
NM_001199040.2:c.2002G>T NP_001185969.1:p.Gly668Trp
NM_001199041.2:c.1936G>T NP_001185970.1:p.Gly646Trp