Canonical Allele Identifier: CA1919905119

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74094225T= , CM000672.2:g.74094225T=	GRCh38
NC_000010.10:g.75853983T= , CM000672.1:g.75853983T=	GRCh37
NC_000010.9:g.75523989T=	NCBI36
NG_008868.1:g.101112T= , LRG_383:g.101112T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1353-46T= MANE Select	ENSP00000211998.5:n.1353-46T=
ENST00000211998.8:c.1353-46T=	ENSP00000211998.4:n.1353-46T=
ENST00000372755.7:c.1353-46T=	ENSP00000361841.3:n.1353-46T=
ENST00000436396.1:c.369-46T=	ENSP00000415489.1:n.369-46T=
ENST00000478896.2:n.332-6829T=
ENST00000623461.3:n.4156-46T=
ENST00000624354.3:c.*1108-46T=	ENSP00000485551.1:n.*1108-46T=
NM_003373.3:c.1353-46T=	NP_003364.1:n.1353-46T=
NM_014000.2:c.1353-46T= , LRG_383t1:c.1353-46T=	NP_054706.1:n.1353-46T=
XM_005270142.1:c.1356-46T=	XP_005270199.1:n.1356-46T=
XM_005270143.1:c.1356-46T=	XP_005270200.1:n.1356-46T=
NM_003373.4:c.1353-46T=	NP_003364.1:n.1353-46T=
NM_014000.3:c.1353-46T= MANE Select	NP_054706.1:n.1353-46T=