Canonical Allele Identifier: CA377268197

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75834503A>C (hg19) ; chr10:g.74074745A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74074745A>C , CM000672.2:g.74074745A>C	GRCh38
NC_000010.10:g.75834503A>C , CM000672.1:g.75834503A>C	GRCh37
NC_000010.9:g.75504509A>C	NCBI36
NG_008868.1:g.81632A>C , LRG_383:g.81632A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.625A>C MANE Select	ENSP00000211998.5:p.Met209Leu
ENST00000211998.8:c.625A>C	ENSP00000211998.4:p.Met209Leu
ENST00000372755.7:c.625A>C	ENSP00000361841.3:p.Met209Leu
ENST00000478896.2:n.332-26309A>C
ENST00000623461.3:n.583A>C
ENST00000624354.3:c.*380A>C	ENSP00000485551.1:n.*380A>C
NM_003373.3:c.625A>C	NP_003364.1:p.Met209Leu
NM_014000.2:c.625A>C , LRG_383t1:c.625A>C	NP_054706.1:p.Met209Leu
XM_005270142.1:c.625A>C	XP_005270199.1:p.Met209Leu
XM_005270143.1:c.625A>C	XP_005270200.1:p.Met209Leu
NM_003373.4:c.625A>C	NP_003364.1:p.Met209Leu
NM_014000.3:c.625A>C MANE Select	NP_054706.1:p.Met209Leu