Canonical Allele Identifier: CA470164035

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75867005C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74107247C>T , CM000672.2:g.74107247C>T	GRCh38
NC_000010.10:g.75867005C>T , CM000672.1:g.75867005C>T	GRCh37
NC_000010.9:g.75537011C>T	NCBI36
NG_008868.1:g.114134C>T , LRG_383:g.114134C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2452C>T MANE Select	ENSP00000211998.5:p.Leu818=
ENST00000211998.8:c.2452C>T	ENSP00000211998.4:p.Leu818=
ENST00000372755.7:c.2452C>T	ENSP00000361841.3:p.Leu818=
ENST00000436396.1:c.1468C>T	ENSP00000415489.1:p.Leu490=
ENST00000472585.1:n.444C>T
ENST00000623461.3:n.5255C>T
ENST00000624354.3:c.*2207C>T	ENSP00000485551.1:n.*2207C>T
NM_003373.3:c.2452C>T	NP_003364.1:p.Leu818=
NM_014000.2:c.2452C>T , LRG_383t1:c.2452C>T	NP_054706.1:p.Leu818=
XM_005270142.1:c.2455C>T	XP_005270199.1:p.Leu819=
XM_005270143.1:c.2455C>T	XP_005270200.1:p.Leu819=
NM_003373.4:c.2452C>T	NP_003364.1:p.Leu818=
NM_014000.3:c.2452C>T MANE Select	NP_054706.1:p.Leu818=