Canonical Allele Identifier: CA470164081

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75867031A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74107273A>C , CM000672.2:g.74107273A>C	GRCh38
NC_000010.10:g.75867031A>C , CM000672.1:g.75867031A>C	GRCh37
NC_000010.9:g.75537037A>C	NCBI36
NG_008868.1:g.114160A>C , LRG_383:g.114160A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.2478A>C MANE Select	ENSP00000211998.5:p.Gly826=
ENST00000211998.8:c.2478A>C	ENSP00000211998.4:p.Gly826=
ENST00000372755.7:c.2478A>C	ENSP00000361841.3:p.Gly826=
ENST00000436396.1:c.1494A>C	ENSP00000415489.1:p.Gly498=
ENST00000472585.1:n.470A>C
ENST00000623461.3:n.5281A>C
ENST00000624354.3:c.*2233A>C	ENSP00000485551.1:n.*2233A>C
NM_003373.3:c.2478A>C	NP_003364.1:p.Gly826=
NM_014000.2:c.2478A>C , LRG_383t1:c.2478A>C	NP_054706.1:p.Gly826=
XM_005270142.1:c.2481A>C	XP_005270199.1:p.Gly827=
XM_005270143.1:c.2481A>C	XP_005270200.1:p.Gly827=
NM_003373.4:c.2478A>C	NP_003364.1:p.Gly826=
NM_014000.3:c.2478A>C MANE Select	NP_054706.1:p.Gly826=