Canonical Allele Identifier: CA2013874066
Gene: VWF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6021881_6021882delinsAC , CM000674.2:g.6021881_6021882delinsAC GRCh38
NC_000012.11:g.6131047_6131048delinsAC , CM000674.1:g.6131047_6131048delinsAC GRCh37
NC_000012.10:g.6001308_6001309delinsAC NCBI36
NG_009072.1:g.107789_107790delinsGT
NG_009072.2:g.107789_107790delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.3674+18_3674+19delinsGT MANE Select ENSP00000261405.5:n.3674+18_3674+19delins...
ENST00000261405.9:c.3674+18_3674+19delinsGT ENSP00000261405.5:n.3674+18_3674+19delins...
ENST00000538635.5:n.421-27948_421-27947delinsGT
ENST00000539641.1:n.27+18_27+19delinsGT
NM_000552.3:c.3674+18_3674+19delinsGT NP_000543.2:n.3674+18_3674+19delinsGT
NM_000552.4:c.3674+18_3674+19delinsGT NP_000543.2:n.3674+18_3674+19delinsGT
NM_000552.5:c.3674+18_3674+19delinsGT MANE Select NP_000543.3:n.3674+18_3674+19delinsGT
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