Canonical Allele Identifier: CA1919902958

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74089213C= , CM000672.2:g.74089213C=	GRCh38
NC_000010.10:g.75848971C= , CM000672.1:g.75848971C=	GRCh37
NC_000010.9:g.75518977C=	NCBI36
NG_008868.1:g.96100C= , LRG_383:g.96100C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1040C= MANE Select	ENSP00000211998.5:p.Pro347=
ENST00000211998.8:c.1040C=	ENSP00000211998.4:p.Pro347=
ENST00000372755.7:c.1040C=	ENSP00000361841.3:p.Pro347=
ENST00000436396.1:c.56C=	ENSP00000415489.1:p.Pro19=
ENST00000478896.2:n.332-11841C=
ENST00000623461.3:n.3843C=
ENST00000624354.3:c.*795C=	ENSP00000485551.1:n.*795C=
NM_003373.3:c.1040C=	NP_003364.1:p.Pro347=
NM_014000.2:c.1040C= , LRG_383t1:c.1040C=	NP_054706.1:p.Pro347=
XM_005270142.1:c.1043C=	XP_005270199.1:p.Pro348=
XM_005270143.1:c.1043C=	XP_005270200.1:p.Pro348=
XR_001747501.1:n.89+719G=
NM_003373.4:c.1040C=	NP_003364.1:p.Pro347=
NM_014000.3:c.1040C= MANE Select	NP_054706.1:p.Pro347=