Canonical Allele Identifier: CA1919906793

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74114349C= , CM000672.2:g.74114349C=	GRCh38
NC_000010.10:g.75874107C= , CM000672.1:g.75874107C=	GRCh37
NC_000010.9:g.75544113C=	NCBI36
NG_008868.1:g.121236C= , LRG_383:g.121236C=

Transcript Alleles

HGVS	Amino-acid Change
NM_014000.3:c.3115C= MANE Select	NP_054706.1:p.Gln1039=
ENST00000211998.10:c.3115C= MANE Select	ENSP00000211998.5:p.Gln1039=
NM_003373.3:c.2911C=	NP_003364.1:p.Gln971=
NM_003373.4:c.2911C=	NP_003364.1:p.Gln971=
NM_014000.2:c.3115C= , LRG_383t1:c.3115C=	NP_054706.1:p.Gln1039=
ENST00000211998.8:c.3115C=	ENSP00000211998.4:p.Gln1039=
ENST00000372755.7:c.2911C=	ENSP00000361841.3:p.Gln971=
ENST00000436396.1:c.2131C=	ENSP00000415489.1:p.Gln711=
ENST00000623461.3:n.5714C=
ENST00000624354.3:c.*2870C=	ENSP00000485551.1:n.*2870C=
XM_005270142.1:c.3118C=	XP_005270199.1:p.Gln1040=
XM_005270143.1:c.2914C=	XP_005270200.1:p.Gln972=