Canonical Allele Identifier: CA470165639

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75871820C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112062C>T , CM000672.2:g.74112062C>T	GRCh38
NC_000010.10:g.75871820C>T , CM000672.1:g.75871820C>T	GRCh37
NC_000010.9:g.75541826C>T	NCBI36
NG_008868.1:g.118949C>T , LRG_383:g.118949C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.2899C>T MANE Select	ENSP00000211998.5:p.Leu967=
ENST00000211998.8:c.2899C>T	ENSP00000211998.4:p.Leu967=
ENST00000372755.7:c.2746-2122C>T	ENSP00000361841.3:n.2746-2122C>T
ENST00000436396.1:c.1915C>T	ENSP00000415489.1:p.Leu639=
ENST00000623461.3:n.5549-2122C>T
ENST00000624354.3:c.*2654C>T	ENSP00000485551.1:n.*2654C>T
NM_003373.3:c.2746-2122C>T	NP_003364.1:n.2746-2122C>T
NM_014000.2:c.2899C>T , LRG_383t1:c.2899C>T	NP_054706.1:p.Leu967=
XM_005270142.1:c.2902C>T	XP_005270199.1:p.Leu968=
XM_005270143.1:c.2749-2122C>T	XP_005270200.1:n.2749-2122C>T
NM_003373.4:c.2746-2122C>T	NP_003364.1:n.2746-2122C>T
NM_014000.3:c.2899C>T MANE Select	NP_054706.1:p.Leu967=