Canonical Allele Identifier: CA2581563856

Gene: VWA7

Genomic Alleles

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

Transcript Alleles

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