Canonical Allele Identifier: CA470171394

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75842301A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082543A>T , CM000672.2:g.74082543A>T	GRCh38
NC_000010.10:g.75842301A>T , CM000672.1:g.75842301A>T	GRCh37
NC_000010.9:g.75512307A>T	NCBI36
NG_008868.1:g.89430A>T , LRG_383:g.89430A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.873A>T MANE Select	ENSP00000211998.5:p.Pro291=
ENST00000211998.8:c.873A>T	ENSP00000211998.4:p.Pro291=
ENST00000372755.7:c.873A>T	ENSP00000361841.3:p.Pro291=
ENST00000478896.2:n.332-18511A>T
ENST00000623461.3:n.3676A>T
ENST00000624354.3:c.*628A>T	ENSP00000485551.1:n.*628A>T
NM_003373.3:c.873A>T	NP_003364.1:p.Pro291=
NM_014000.2:c.873A>T , LRG_383t1:c.873A>T	NP_054706.1:p.Pro291=
XM_005270142.1:c.876A>T	XP_005270199.1:p.Pro292=
XM_005270143.1:c.876A>T	XP_005270200.1:p.Pro292=
XR_001747501.1:n.90-4816T>A
NM_003373.4:c.873A>T	NP_003364.1:p.Pro291=
NM_014000.3:c.873A>T MANE Select	NP_054706.1:p.Pro291=