Canonical Allele Identifier: CA7655169

Gene: STRA6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74207712C>T , CM000677.2:g.74207712C>T	GRCh38
NC_000015.9:g.74500053C>T , CM000677.1:g.74500053C>T	GRCh37
NC_000015.8:g.72287106C>T	NCBI36
NG_009207.1:g.6319G>A
NG_054754.1:g.10008C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558645.5:n.90-1676C>T
ENST00000560148.5:n.395-1676C>T
ENST00000561332.1:n.50-1676C>T
ENST00000323940.9:c.-16+1088G>A	ENSP00000326085.5:n.-16+1088G>A
ENST00000416286.7:c.-16+4415G>A	ENSP00000400403.3:n.-16+4415G>A
ENST00000423167.6:c.-16+1088G>A	ENSP00000413012.2:n.-16+1088G>A
ENST00000432245.6:c.-16+1088G>A	ENSP00000407176.2:n.-16+1088G>A
ENST00000449139.6:c.-16+4415G>A	ENSP00000410221.2:n.-16+4415G>A
ENST00000535552.5:c.96+1647G>A	ENSP00000440238.1:n.96+1647G>A
ENST00000574278.5:c.15G>A	ENSP00000458827.1:p.Gly5=
NM_001142617.1:c.-16+1088G>A	NP_001136089.1:n.-16+1088G>A
NM_001142619.1:c.-16+1088G>A	NP_001136091.1:n.-16+1088G>A
NM_001142620.1:c.-16+1088G>A	NP_001136092.1:n.-16+1088G>A
NM_001199040.1:c.96+1647G>A	NP_001185969.1:n.96+1647G>A
NM_001199041.1:c.15G>A	NP_001185970.1:p.Gly5=
XM_011521883.1:c.-16+4415G>A	XP_011520185.1:n.-16+4415G>A
XM_017022479.1:c.-48+4415G>A	XP_016877968.1:n.-48+4415G>A
NM_001142617.2:c.-16+1088G>A	NP_001136089.1:n.-16+1088G>A
NM_001142619.2:c.-16+1088G>A	NP_001136091.1:n.-16+1088G>A
NM_001142620.2:c.-16+1088G>A	NP_001136092.1:n.-16+1088G>A
NM_001199040.2:c.96+1647G>A	NP_001185969.1:n.96+1647G>A
NM_001199041.2:c.15G>A	NP_001185970.1:p.Gly5=