Canonical Allele Identifier: CA2788549049

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119400A>C , CM000672.2:g.74119400A>C	GRCh38
NC_000010.10:g.75879158A>C , CM000672.1:g.75879158A>C	GRCh37
NC_000010.9:g.75549164A>C	NCBI36
NG_008868.1:g.126287A>C , LRG_383:g.126287A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1231A>C MANE Select	ENSP00000211998.5:n.*1231A>C
ENST00000211998.8:c.*1231A>C	ENSP00000211998.4:n.*1231A>C
ENST00000372755.7:c.*1231A>C	ENSP00000361841.3:n.*1231A>C
ENST00000436396.1:c.3652A>C	ENSP00000415489.1:n.3652A>C
ENST00000623461.3:n.7235A>C
NM_003373.3:c.*1231A>C	NP_003364.1:n.*1231A>C
NM_014000.2:c.*1231A>C , LRG_383t1:c.*1231A>C	NP_054706.1:n.*1231A>C
XM_005270142.1:c.*1231A>C	XP_005270199.1:n.*1231A>C
XM_005270143.1:c.*1231A>C	XP_005270200.1:n.*1231A>C
NM_003373.4:c.*1231A>C	NP_003364.1:n.*1231A>C
NM_014000.3:c.*1231A>C MANE Select	NP_054706.1:n.*1231A>C