Canonical Allele Identifier: CA1619300227

Gene: VWA7

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31774813A>T , CM000668.2:g.31774813A>T	GRCh38
NC_000006.11:g.31742590A>T , CM000668.1:g.31742590A>T	GRCh37
NC_000006.10:g.31850569A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375688.5:c.611-187T>A MANE Select	ENSP00000364840.4:n.611-187T>A
ENST00000375688.4:c.611-187T>A	ENSP00000364840.4:n.611-187T>A
ENST00000467576.1:n.590-187T>A
NM_025258.2:c.611-187T>A	NP_079534.2:n.611-187T>A
XM_005249427.1:c.611-187T>A	XP_005249484.1:n.611-187T>A
XR_926313.1:n.849-187T>A
XM_005249427.2:c.611-187T>A	XP_005249484.1:n.611-187T>A
XM_017011327.2:c.611-187T>A	XP_016866816.1:n.611-187T>A
XM_017011328.1:c.611-187T>A	XP_016866817.1:n.611-187T>A
XM_017011329.1:c.-231-187T>A	XP_016866818.1:n.-231-187T>A
XR_001743651.2:n.911-187T>A
NM_025258.3:c.611-187T>A MANE Select	NP_079534.2:n.611-187T>A