Canonical Allele Identifier: CA491171454

Gene: STRA6

Linked Data

• gnomAD v4: 15-74181422-G-A
• MyVariant Identifiers: chr15:g.74473763G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74181422G>A , CM000677.2:g.74181422G>A	GRCh38
NC_000015.9:g.74473763G>A , CM000677.1:g.74473763G>A	GRCh37
NC_000015.8:g.72260816G>A	NCBI36
NG_009207.1:g.32609C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1557C>T MANE Select	ENSP00000378537.4:p.Pro519=
ENST00000323940.9:c.1557C>T	ENSP00000326085.5:p.Pro519=
ENST00000395105.8:c.1557C>T	ENSP00000378537.4:p.Pro519=
ENST00000416286.7:c.1533C>T	ENSP00000400403.3:p.Pro511=
ENST00000423167.6:c.1530C>T	ENSP00000413012.2:p.Pro510=
ENST00000449139.6:c.1557C>T	ENSP00000410221.2:p.Pro519=
ENST00000535552.5:c.1668C>T	ENSP00000440238.1:p.Pro556=
ENST00000545137.5:n.1266C>T
ENST00000563965.5:c.1674C>T	ENSP00000456609.1:p.Pro558=
ENST00000572785.1:c.412C>T
ENST00000574278.5:c.1602C>T	ENSP00000458827.1:p.Pro534=
ENST00000574439.5:n.1829C>T
ENST00000616000.4:c.1557C>T	ENSP00000479112.1:p.Pro519=
NM_001142617.1:c.1557C>T	NP_001136089.1:p.Pro519=
NM_001142618.1:c.1557C>T	NP_001136090.1:p.Pro519=
NM_001142619.1:c.1530C>T	NP_001136091.1:p.Pro510=
NM_001199040.1:c.1668C>T	NP_001185969.1:p.Pro556=
NM_001199041.1:c.1602C>T	NP_001185970.1:p.Pro534=
NM_001199042.1:c.1674C>T	NP_001185971.1:p.Pro558=
NM_022369.3:c.1557C>T	NP_071764.3:p.Pro519=
XM_011521883.1:c.1557C>T	XP_011520185.1:p.Pro519=
XM_011521884.1:c.1368C>T	XP_011520186.1:p.Pro456=
XM_017022478.1:c.1605C>T	XP_016877967.1:p.Pro535=
XM_017022479.1:c.1557C>T	XP_016877968.1:p.Pro519=
XM_017022480.1:c.1368C>T	XP_016877969.1:p.Pro456=
NM_022369.4:c.1557C>T MANE Select	NP_071764.3:p.Pro519=
NM_001142617.2:c.1557C>T	NP_001136089.1:p.Pro519=
NM_001142619.2:c.1530C>T	NP_001136091.1:p.Pro510=
NM_001199042.2:c.1674C>T	NP_001185971.1:p.Pro558=
NM_001142618.2:c.1557C>T	NP_001136090.1:p.Pro519=
NM_001199040.2:c.1668C>T	NP_001185969.1:p.Pro556=
NM_001199041.2:c.1602C>T	NP_001185970.1:p.Pro534=