Canonical Allele Identifier: CA1919905833

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112122A= , CM000672.2:g.74112122A=	GRCh38
NC_000010.10:g.75871880A= , CM000672.1:g.75871880A=	GRCh37
NC_000010.9:g.75541886A=	NCBI36
NG_008868.1:g.119009A= , LRG_383:g.119009A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2949+10A= MANE Select	ENSP00000211998.5:n.2949+10A=
ENST00000211998.8:c.2949+10A=	ENSP00000211998.4:n.2949+10A=
ENST00000372755.7:c.2746-2062A=	ENSP00000361841.3:n.2746-2062A=
ENST00000436396.1:c.1965+10A=	ENSP00000415489.1:n.1965+10A=
ENST00000623461.3:n.5549-2062A=
ENST00000624354.3:c.*2704+10A=	ENSP00000485551.1:n.*2704+10A=
NM_003373.3:c.2746-2062A=	NP_003364.1:n.2746-2062A=
NM_014000.2:c.2949+10A= , LRG_383t1:c.2949+10A=	NP_054706.1:n.2949+10A=
XM_005270142.1:c.2952+10A=	XP_005270199.1:n.2952+10A=
XM_005270143.1:c.2749-2062A=	XP_005270200.1:n.2749-2062A=
NM_003373.4:c.2746-2062A=	NP_003364.1:n.2746-2062A=
NM_014000.3:c.2949+10A= MANE Select	NP_054706.1:n.2949+10A=