Canonical Allele Identifier: CA2013874168

Gene: VWF

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6022123_6022145delinsCCTCCTCCTGCCCTAGAAGCCAA , CM000674.2:g.6022123_6022145delinsCCTCCTCCTGCCCTAGAAGCCAA	GRCh38
NC_000012.11:g.6131289_6131311delinsCCTCCTCCTGCCCTAGAAGCCAA , CM000674.1:g.6131289_6131311delinsCCTCCTCCTGCCCTAGAAGCCAA	GRCh37
NC_000012.10:g.6001550_6001572delinsCCTCCTCCTGCCCTAGAAGCCAA	NCBI36
NG_009072.1:g.107526_107548delinsTTGGCTTCTAGGGCAGGAGGAGG
NG_009072.2:g.107526_107548delinsTTGGCTTCTAGGGCAGGAGGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAGGAGG MANE Select	ENSP00000261405.5:n.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAG...
ENST00000261405.9:c.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAGGAGG	ENSP00000261405.5:n.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAG...
ENST00000538635.5:n.421-28211_421-28189delinsTTGGCTTCTAGGGCAGGAGGAGG
NM_000552.3:c.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAGGAGG	NP_000543.2:n.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAGGAGG
NM_000552.4:c.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAGGAGG	NP_000543.2:n.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAGGAGG
NM_000552.5:c.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAGGAGG MANE Select	NP_000543.3:n.3539-110_3539-88delinsTTGGCTTCTAGGGCAGGAGGAGG