Canonical Allele Identifier: CA1919889767

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74070824G= , CM000672.2:g.74070824G=	GRCh38
NC_000010.10:g.75830582G= , CM000672.1:g.75830582G=	GRCh37
NC_000010.9:g.75500588G=	NCBI36
NG_008868.1:g.77711G= , LRG_383:g.77711G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.390+4G= MANE Select	ENSP00000211998.5:n.390+4G=
ENST00000211998.8:c.390+4G=	ENSP00000211998.4:n.390+4G=
ENST00000372755.7:c.390+4G=	ENSP00000361841.3:n.390+4G=
ENST00000478896.2:n.331+27671G=
ENST00000623461.3:n.348+4G=
ENST00000624354.3:c.*145+4G=	ENSP00000485551.1:n.*145+4G=
NM_003373.3:c.390+4G=	NP_003364.1:n.390+4G=
NM_014000.2:c.390+4G= , LRG_383t1:c.390+4G=	NP_054706.1:n.390+4G=
XM_005270142.1:c.390+4G=	XP_005270199.1:n.390+4G=
XM_005270143.1:c.390+4G=	XP_005270200.1:n.390+4G=
NM_003373.4:c.390+4G=	NP_003364.1:n.390+4G=
NM_014000.3:c.390+4G= MANE Select	NP_054706.1:n.390+4G=