Canonical Allele Identifier: CA377264828

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75871817A>T (hg19) ; chr10:g.74112059A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112059A>T , CM000672.2:g.74112059A>T	GRCh38
NC_000010.10:g.75871817A>T , CM000672.1:g.75871817A>T	GRCh37
NC_000010.9:g.75541823A>T	NCBI36
NG_008868.1:g.118946A>T , LRG_383:g.118946A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2896A>T MANE Select	ENSP00000211998.5:p.Ile966Phe
ENST00000211998.8:c.2896A>T	ENSP00000211998.4:p.Ile966Phe
ENST00000372755.7:c.2746-2125A>T	ENSP00000361841.3:n.2746-2125A>T
ENST00000436396.1:c.1912A>T	ENSP00000415489.1:p.Ile638Phe
ENST00000623461.3:n.5549-2125A>T
ENST00000624354.3:c.*2651A>T	ENSP00000485551.1:n.*2651A>T
NM_003373.3:c.2746-2125A>T	NP_003364.1:n.2746-2125A>T
NM_014000.2:c.2896A>T , LRG_383t1:c.2896A>T	NP_054706.1:p.Ile966Phe
XM_005270142.1:c.2899A>T	XP_005270199.1:p.Ile967Phe
XM_005270143.1:c.2749-2125A>T	XP_005270200.1:n.2749-2125A>T
NM_003373.4:c.2746-2125A>T	NP_003364.1:n.2746-2125A>T
NM_014000.3:c.2896A>T MANE Select	NP_054706.1:p.Ile966Phe