Canonical Allele Identifier: CA2640215076

Gene: CANT1

Linked Data

• gnomAD v4: 17-78995233-G-GCTCTAACCGGGGTGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78995233_78995234insCTCTAACCGGGGTGAC , CM000679.2:g.78995233_78995234insCTCTAACCGGGGTGAC	GRCh38
NC_000017.10:g.76991315_76991316insCTCTAACCGGGGTGAC , CM000679.1:g.76991315_76991316insCTCTAACCGGGGTGAC	GRCh37
NC_000017.9:g.74502910_74502911insCTCTAACCGGGGTGAC	NCBI36
NG_016645.1:g.19584_19585insGTCACCCCGGTTAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392446.10:c.632-13_632-12insGTCACCCCGGTTAGAG MANE Select	ENSP00000376241.4:n.632-13_632-12insGTCACCCCGGTTAGAG
ENST00000302345.6:c.632-13_632-12insGTCACCCCGGTTAGAG	ENSP00000307674.2:n.632-13_632-12insGTCACCCCGGTTAGAG
ENST00000392446.9:c.632-13_632-12insGTCACCCCGGTTAGAG	ENSP00000376241.4:n.632-13_632-12insGTCACCCCGGTTAGAG
ENST00000588096.1:n.16_17insGTCACCCCGGTTAGAG
ENST00000591773.5:c.632-13_632-12insGTCACCCCGGTTAGAG	ENSP00000467437.1:n.632-13_632-12insGTCACCCCGGTTAGAG
ENST00000592228.1:c.647+1742_647+1743insGTCACCCCGGTTAGAG	ENSP00000466743.1:n.647+1742_647+1743insGTCACCCCGGTTAGAG
ENST00000620915.4:c.632-13_632-12insGTCACCCCGGTTAGAG	ENSP00000477798.1:n.632-13_632-12insGTCACCCCGGTTAGAG
NM_001159772.1:c.632-13_632-12insGTCACCCCGGTTAGAG	NP_001153244.1:n.632-13_632-12insGTCACCCCGGTTAGAG
NM_001159773.1:c.632-13_632-12insGTCACCCCGGTTAGAG	NP_001153245.1:n.632-13_632-12insGTCACCCCGGTTAGAG
NM_138793.3:c.632-13_632-12insGTCACCCCGGTTAGAG	NP_620148.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_005257020.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_005257077.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_005257021.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_005257078.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_005257022.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_005257079.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_006721683.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_006721746.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_011524291.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_011522593.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_011524292.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_011522594.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_011524293.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_011522595.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_011524294.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_011522596.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_011524295.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_011522597.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_011524294.2:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_011522596.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_011524295.2:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_011522597.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XM_024450564.1:c.632-13_632-12insGTCACCCCGGTTAGAG	XP_024306332.1:n.632-13_632-12insGTCACCCCGGTTAGAG
XR_001752424.2:n.1076-13_1076-12insGTCACCCCGGTTAGAG
NM_001159773.2:c.632-13_632-12insGTCACCCCGGTTAGAG MANE Select	NP_001153245.1:n.632-13_632-12insGTCACCCCGGTTAGAG
NM_001159772.2:c.632-13_632-12insGTCACCCCGGTTAGAG	NP_001153244.1:n.632-13_632-12insGTCACCCCGGTTAGAG
NM_138793.4:c.632-13_632-12insGTCACCCCGGTTAGAG	NP_620148.1:n.632-13_632-12insGTCACCCCGGTTAGAG