Canonical Allele Identifier: CA377266798

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75830827A>T (hg19) ; chr10:g.74071069A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071069A>T , CM000672.2:g.74071069A>T	GRCh38
NC_000010.10:g.75830827A>T , CM000672.1:g.75830827A>T	GRCh37
NC_000010.9:g.75500833A>T	NCBI36
NG_008868.1:g.77956A>T , LRG_383:g.77956A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.485A>T MANE Select	ENSP00000211998.5:p.Lys162Met
ENST00000211998.8:c.485A>T	ENSP00000211998.4:p.Lys162Met
ENST00000372755.7:c.485A>T	ENSP00000361841.3:p.Lys162Met
ENST00000478896.2:n.331+27916A>T
ENST00000623461.3:n.443A>T
ENST00000624354.3:c.*240A>T	ENSP00000485551.1:n.*240A>T
NM_003373.3:c.485A>T	NP_003364.1:p.Lys162Met
NM_014000.2:c.485A>T , LRG_383t1:c.485A>T	NP_054706.1:p.Lys162Met
XM_005270142.1:c.485A>T	XP_005270199.1:p.Lys162Met
XM_005270143.1:c.485A>T	XP_005270200.1:p.Lys162Met
NM_003373.4:c.485A>T	NP_003364.1:p.Lys162Met
NM_014000.3:c.485A>T MANE Select	NP_054706.1:p.Lys162Met