Canonical Allele Identifier: CA401307269

Gene: CANT1

Linked Data

• MyVariant Identifiers: chr17:g.76991238A>G (hg19) ; chr17:g.78995156A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78995156A>G , CM000679.2:g.78995156A>G	GRCh38
NC_000017.10:g.76991238A>G , CM000679.1:g.76991238A>G	GRCh37
NC_000017.9:g.74502833A>G	NCBI36
NG_016645.1:g.19662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392446.10:c.697T>C MANE Select	ENSP00000376241.4:p.Trp233Arg
ENST00000302345.6:c.697T>C	ENSP00000307674.2:p.Trp233Arg
ENST00000392446.9:c.697T>C	ENSP00000376241.4:p.Trp233Arg
ENST00000588096.1:n.94T>C
ENST00000591773.5:c.697T>C	ENSP00000467437.1:p.Trp233Arg
ENST00000592228.1:c.647+1820T>C	ENSP00000466743.1:n.647+1820T>C
ENST00000620915.4:c.697T>C	ENSP00000477798.1:p.Trp233Arg
NM_001159772.1:c.697T>C	NP_001153244.1:p.Trp233Arg
NM_001159773.1:c.697T>C	NP_001153245.1:p.Trp233Arg
NM_138793.3:c.697T>C	NP_620148.1:p.Trp233Arg
XM_005257020.1:c.697T>C	XP_005257077.1:p.Trp233Arg
XM_005257021.1:c.697T>C	XP_005257078.1:p.Trp233Arg
XM_005257022.1:c.697T>C	XP_005257079.1:p.Trp233Arg
XM_006721683.1:c.697T>C	XP_006721746.1:p.Trp233Arg
XM_011524291.1:c.697T>C	XP_011522593.1:p.Trp233Arg
XM_011524292.1:c.697T>C	XP_011522594.1:p.Trp233Arg
XM_011524293.1:c.697T>C	XP_011522595.1:p.Trp233Arg
XM_011524294.1:c.697T>C	XP_011522596.1:p.Trp233Arg
XM_011524295.1:c.697T>C	XP_011522597.1:p.Trp233Arg
XM_011524294.2:c.697T>C	XP_011522596.1:p.Trp233Arg
XM_011524295.2:c.697T>C	XP_011522597.1:p.Trp233Arg
XM_024450564.1:c.697T>C	XP_024306332.1:p.Trp233Arg
XR_001752424.2:n.1141T>C
NM_001159773.2:c.697T>C MANE Select	NP_001153245.1:p.Trp233Arg
NM_001159772.2:c.697T>C	NP_001153244.1:p.Trp233Arg
NM_138793.4:c.697T>C	NP_620148.1:p.Trp233Arg