Canonical Allele Identifier: CA1919905847

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112150T= , CM000672.2:g.74112150T=	GRCh38
NC_000010.10:g.75871908T= , CM000672.1:g.75871908T=	GRCh37
NC_000010.9:g.75541914T=	NCBI36
NG_008868.1:g.119037T= , LRG_383:g.119037T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2949+38T= MANE Select	ENSP00000211998.5:n.2949+38T=
ENST00000211998.8:c.2949+38T=	ENSP00000211998.4:n.2949+38T=
ENST00000372755.7:c.2746-2034T=	ENSP00000361841.3:n.2746-2034T=
ENST00000436396.1:c.1965+38T=	ENSP00000415489.1:n.1965+38T=
ENST00000623461.3:n.5549-2034T=
ENST00000624354.3:c.*2704+38T=	ENSP00000485551.1:n.*2704+38T=
NM_003373.3:c.2746-2034T=	NP_003364.1:n.2746-2034T=
NM_014000.2:c.2949+38T= , LRG_383t1:c.2949+38T=	NP_054706.1:n.2949+38T=
XM_005270142.1:c.2952+38T=	XP_005270199.1:n.2952+38T=
XM_005270143.1:c.2749-2034T=	XP_005270200.1:n.2749-2034T=
NM_003373.4:c.2746-2034T=	NP_003364.1:n.2746-2034T=
NM_014000.3:c.2949+38T= MANE Select	NP_054706.1:n.2949+38T=