Canonical Allele Identifier: CA2575054127

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6058137_6058138insAG , CM000674.2:g.6058137_6058138insAG	GRCh38
NC_000012.11:g.6167303_6167304insAG , CM000674.1:g.6167303_6167304insAG	GRCh37
NC_000012.10:g.6037564_6037565insAG	NCBI36
NG_009072.1:g.71533_71534insCT
NG_009072.2:g.71533_71534insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.1534-94_1534-93insCT MANE Select	ENSP00000261405.5:n.1534-94_1534-93insCT
ENST00000261405.9:c.1534-94_1534-93insCT	ENSP00000261405.5:n.1534-94_1534-93insCT
ENST00000538635.5:n.420+52377_420+52378insCT
NM_000552.3:c.1534-94_1534-93insCT	NP_000543.2:n.1534-94_1534-93insCT
NM_000552.4:c.1534-94_1534-93insCT	NP_000543.2:n.1534-94_1534-93insCT
NM_000552.5:c.1534-94_1534-93insCT MANE Select	NP_000543.3:n.1534-94_1534-93insCT