Canonical Allele Identifier: CA470164031

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75867004C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74107246C>T , CM000672.2:g.74107246C>T	GRCh38
NC_000010.10:g.75867004C>T , CM000672.1:g.75867004C>T	GRCh37
NC_000010.9:g.75537010C>T	NCBI36
NG_008868.1:g.114133C>T , LRG_383:g.114133C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2451C>T MANE Select	ENSP00000211998.5:p.Phe817=
ENST00000211998.8:c.2451C>T	ENSP00000211998.4:p.Phe817=
ENST00000372755.7:c.2451C>T	ENSP00000361841.3:p.Phe817=
ENST00000436396.1:c.1467C>T	ENSP00000415489.1:p.Phe489=
ENST00000472585.1:n.443C>T
ENST00000623461.3:n.5254C>T
ENST00000624354.3:c.*2206C>T	ENSP00000485551.1:n.*2206C>T
NM_003373.3:c.2451C>T	NP_003364.1:p.Phe817=
NM_014000.2:c.2451C>T , LRG_383t1:c.2451C>T	NP_054706.1:p.Phe817=
XM_005270142.1:c.2454C>T	XP_005270199.1:p.Phe818=
XM_005270143.1:c.2454C>T	XP_005270200.1:p.Phe818=
NM_003373.4:c.2451C>T	NP_003364.1:p.Phe817=
NM_014000.3:c.2451C>T MANE Select	NP_054706.1:p.Phe817=