Canonical Allele Identifier: CA1630848366

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74107171C= , CM000672.2:g.74107171C=	GRCh38
NC_000010.10:g.75866929C= , CM000672.1:g.75866929C=	GRCh37
NC_000010.9:g.75536935C=	NCBI36
NG_008868.1:g.114058C= , LRG_383:g.114058C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2435-59C= MANE Select	ENSP00000211998.5:n.2435-59C=
ENST00000211998.8:c.2435-59C=	ENSP00000211998.4:n.2435-59C=
ENST00000372755.7:c.2435-59C=	ENSP00000361841.3:n.2435-59C=
ENST00000436396.1:c.1451-59C=	ENSP00000415489.1:n.1451-59C=
ENST00000472585.1:n.427-59C=
ENST00000623461.3:n.5238-59C=
ENST00000624354.3:c.*2190-59C=	ENSP00000485551.1:n.*2190-59C=
NM_003373.3:c.2435-59C=	NP_003364.1:n.2435-59C=
NM_014000.2:c.2435-59C= , LRG_383t1:c.2435-59C=	NP_054706.1:n.2435-59C=
XM_005270142.1:c.2438-59C=	XP_005270199.1:n.2438-59C=
XM_005270143.1:c.2438-59C=	XP_005270200.1:n.2438-59C=
NM_003373.4:c.2435-59C=	NP_003364.1:n.2435-59C=
NM_014000.3:c.2435-59C= MANE Select	NP_054706.1:n.2435-59C=