Canonical Allele Identifier: CA1919908952

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119590A= , CM000672.2:g.74119590A=	GRCh38
NC_000010.10:g.75879348A= , CM000672.1:g.75879348A=	GRCh37
NC_000010.9:g.75549354A=	NCBI36
NG_008868.1:g.126477A= , LRG_383:g.126477A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1421A= MANE Select	ENSP00000211998.5:n.*1421A=
ENST00000211998.8:c.*1421A=	ENSP00000211998.4:n.*1421A=
ENST00000372755.7:c.*1421A=	ENSP00000361841.3:n.*1421A=
ENST00000436396.1:c.3842A=	ENSP00000415489.1:n.3842A=
ENST00000623461.3:n.7425A=
NM_003373.3:c.*1421A=	NP_003364.1:n.*1421A=
NM_014000.2:c.*1421A= , LRG_383t1:c.*1421A=	NP_054706.1:n.*1421A=
XM_005270142.1:c.*1421A=	XP_005270199.1:n.*1421A=
XM_005270143.1:c.*1421A=	XP_005270200.1:n.*1421A=
NM_003373.4:c.*1421A=	NP_003364.1:n.*1421A=
NM_014000.3:c.*1421A= MANE Select	NP_054706.1:n.*1421A=