Canonical Allele Identifier: CA1919890035

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071102C= , CM000672.2:g.74071102C=	GRCh38
NC_000010.10:g.75830860C= , CM000672.1:g.75830860C=	GRCh37
NC_000010.9:g.75500866C=	NCBI36
NG_008868.1:g.77989C= , LRG_383:g.77989C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.499+19C= MANE Select	ENSP00000211998.5:n.499+19C=
ENST00000211998.8:c.499+19C=	ENSP00000211998.4:n.499+19C=
ENST00000372755.7:c.499+19C=	ENSP00000361841.3:n.499+19C=
ENST00000478896.2:n.331+27949C=
ENST00000623461.3:n.457+19C=
ENST00000624354.3:c.*254+19C=	ENSP00000485551.1:n.*254+19C=
NM_003373.3:c.499+19C=	NP_003364.1:n.499+19C=
NM_014000.2:c.499+19C= , LRG_383t1:c.499+19C=	NP_054706.1:n.499+19C=
XM_005270142.1:c.499+19C=	XP_005270199.1:n.499+19C=
XM_005270143.1:c.499+19C=	XP_005270200.1:n.499+19C=
NM_003373.4:c.499+19C=	NP_003364.1:n.499+19C=
NM_014000.3:c.499+19C= MANE Select	NP_054706.1:n.499+19C=