Canonical Allele Identifier: CA2277258780

Gene: CANT1

Linked Data

• dbSNP Id: rs2071001562
• gnomAD v4: 17-78995368-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78995368G>C , CM000679.2:g.78995368G>C	GRCh38
NC_000017.10:g.76991450G>C , CM000679.1:g.76991450G>C	GRCh37
NC_000017.9:g.74503045G>C	NCBI36
NG_016645.1:g.19450C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392446.10:c.632-147C>G MANE Select	ENSP00000376241.4:n.632-147C>G
ENST00000302345.6:c.632-147C>G	ENSP00000307674.2:n.632-147C>G
ENST00000392446.9:c.632-147C>G	ENSP00000376241.4:n.632-147C>G
ENST00000591773.5:c.632-147C>G	ENSP00000467437.1:n.632-147C>G
ENST00000592228.1:c.647+1608C>G	ENSP00000466743.1:n.647+1608C>G
ENST00000620915.4:c.632-147C>G	ENSP00000477798.1:n.632-147C>G
NM_001159772.1:c.632-147C>G	NP_001153244.1:n.632-147C>G
NM_001159773.1:c.632-147C>G	NP_001153245.1:n.632-147C>G
NM_138793.3:c.632-147C>G	NP_620148.1:n.632-147C>G
XM_005257020.1:c.632-147C>G	XP_005257077.1:n.632-147C>G
XM_005257021.1:c.632-147C>G	XP_005257078.1:n.632-147C>G
XM_005257022.1:c.632-147C>G	XP_005257079.1:n.632-147C>G
XM_006721683.1:c.632-147C>G	XP_006721746.1:n.632-147C>G
XM_011524291.1:c.632-147C>G	XP_011522593.1:n.632-147C>G
XM_011524292.1:c.632-147C>G	XP_011522594.1:n.632-147C>G
XM_011524293.1:c.632-147C>G	XP_011522595.1:n.632-147C>G
XM_011524294.1:c.632-147C>G	XP_011522596.1:n.632-147C>G
XM_011524295.1:c.632-147C>G	XP_011522597.1:n.632-147C>G
XM_011524294.2:c.632-147C>G	XP_011522596.1:n.632-147C>G
XM_011524295.2:c.632-147C>G	XP_011522597.1:n.632-147C>G
XM_024450564.1:c.632-147C>G	XP_024306332.1:n.632-147C>G
XR_001752424.2:n.1076-147C>G
NM_001159773.2:c.632-147C>G MANE Select	NP_001153245.1:n.632-147C>G
NM_001159772.2:c.632-147C>G	NP_001153244.1:n.632-147C>G
NM_138793.4:c.632-147C>G	NP_620148.1:n.632-147C>G