Canonical Allele Identifier: CA1619300228

Gene: VWA7

Genomic Alleles

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

Transcript Alleles

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