Canonical Allele Identifier: CA1919898884

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74107239A= , CM000672.2:g.74107239A=	GRCh38
NC_000010.10:g.75866997A= , CM000672.1:g.75866997A=	GRCh37
NC_000010.9:g.75537003A=	NCBI36
NG_008868.1:g.114126A= , LRG_383:g.114126A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2444A= MANE Select	ENSP00000211998.5:p.Lys815=
ENST00000211998.8:c.2444A=	ENSP00000211998.4:p.Lys815=
ENST00000372755.7:c.2444A=	ENSP00000361841.3:p.Lys815=
ENST00000436396.1:c.1460A=	ENSP00000415489.1:p.Lys487=
ENST00000472585.1:n.436A=
ENST00000623461.3:n.5247A=
ENST00000624354.3:c.*2199A=	ENSP00000485551.1:n.*2199A=
NM_003373.3:c.2444A=	NP_003364.1:p.Lys815=
NM_014000.2:c.2444A= , LRG_383t1:c.2444A=	NP_054706.1:p.Lys815=
XM_005270142.1:c.2447A=	XP_005270199.1:p.Lys816=
XM_005270143.1:c.2447A=	XP_005270200.1:p.Lys816=
NM_003373.4:c.2444A=	NP_003364.1:p.Lys815=
NM_014000.3:c.2444A= MANE Select	NP_054706.1:p.Lys815=