Canonical Allele Identifier: CA7654371

Gene: STRA6

Linked Data

• dbSNP Id: rs762100127
• ExAC: 15:74472431 G / T
• gnomAD v2: 15-74472431-G-T
• gnomAD v4: 15-74180090-G-T
• MyVariant Identifiers: chr15:g.74472431G>T (hg19) ; chr15:g.74180090G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180090G>T , CM000677.2:g.74180090G>T	GRCh38
NC_000015.9:g.74472431G>T , CM000677.1:g.74472431G>T	GRCh37
NC_000015.8:g.72259484G>T	NCBI36
NG_009207.1:g.33941C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1994C>A MANE Select	ENSP00000378537.4:p.Ala665Asp
ENST00000323940.9:c.1994C>A	ENSP00000326085.5:p.Ala665Asp
ENST00000395105.8:c.1994C>A	ENSP00000378537.4:p.Ala665Asp
ENST00000416286.7:c.1970C>A	ENSP00000400403.3:p.Ala657Asp
ENST00000423167.6:c.1967C>A	ENSP00000413012.2:p.Ala656Asp
ENST00000449139.6:c.1994C>A	ENSP00000410221.2:p.Ala665Asp
ENST00000535552.5:c.2105C>A	ENSP00000440238.1:p.Ala702Asp
ENST00000545137.5:n.1703C>A
ENST00000563965.5:c.2111C>A	ENSP00000456609.1:p.Ala704Asp
ENST00000574278.5:c.2039C>A	ENSP00000458827.1:p.Ala680Asp
ENST00000574439.5:n.2266C>A
ENST00000616000.4:c.1994C>A	ENSP00000479112.1:p.Ala665Asp
NM_001142617.1:c.1994C>A	NP_001136089.1:p.Ala665Asp
NM_001142618.1:c.1994C>A	NP_001136090.1:p.Ala665Asp
NM_001142619.1:c.1967C>A	NP_001136091.1:p.Ala656Asp
NM_001199040.1:c.2105C>A	NP_001185969.1:p.Ala702Asp
NM_001199041.1:c.2039C>A	NP_001185970.1:p.Ala680Asp
NM_001199042.1:c.2111C>A	NP_001185971.1:p.Ala704Asp
NM_022369.3:c.1994C>A	NP_071764.3:p.Ala665Asp
XM_011521883.1:c.1994C>A	XP_011520185.1:p.Ala665Asp
XM_011521884.1:c.1805C>A	XP_011520186.1:p.Ala602Asp
XM_017022478.1:c.2042C>A	XP_016877967.1:p.Ala681Asp
XM_017022479.1:c.1994C>A	XP_016877968.1:p.Ala665Asp
XM_017022480.1:c.1805C>A	XP_016877969.1:p.Ala602Asp
NM_022369.4:c.1994C>A MANE Select	NP_071764.3:p.Ala665Asp
NM_001142617.2:c.1994C>A	NP_001136089.1:p.Ala665Asp
NM_001142619.2:c.1967C>A	NP_001136091.1:p.Ala656Asp
NM_001199042.2:c.2111C>A	NP_001185971.1:p.Ala704Asp
NM_001142618.2:c.1994C>A	NP_001136090.1:p.Ala665Asp
NM_001199040.2:c.2105C>A	NP_001185969.1:p.Ala702Asp
NM_001199041.2:c.2039C>A	NP_001185970.1:p.Ala680Asp