Canonical Allele Identifier: CA10640808

Gene: CANT1

Linked Data

• ClinVar Variation Id: 325694
• ClinVar RCV Id: RCV000335554
• dbSNP Id: rs146866436
• gnomAD v2: 17-76989543-C-T
• gnomAD v3: 17-78993461-C-T
• gnomAD v4: 17-78993461-C-T
• MyVariant Identifiers: chr17:g.76989543C>T (hg19) ; chr17:g.78993461C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78993461C>T , CM000679.2:g.78993461C>T	GRCh38
NC_000017.10:g.76989543C>T , CM000679.1:g.76989543C>T	GRCh37
NC_000017.9:g.74501138C>T	NCBI36
NG_016645.1:g.21357G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392446.10:c.*89G>A MANE Select	ENSP00000376241.4:n.*89G>A
ENST00000302345.6:c.*89G>A	ENSP00000307674.2:n.*89G>A
ENST00000392446.9:c.*89G>A	ENSP00000376241.4:n.*89G>A
ENST00000592228.1:c.648-700G>A	ENSP00000466743.1:n.648-700G>A
ENST00000620915.4:c.*89G>A	ENSP00000477798.1:n.*89G>A
NM_001159772.1:c.*89G>A	NP_001153244.1:n.*89G>A
NM_001159773.1:c.*89G>A	NP_001153245.1:n.*89G>A
NM_138793.3:c.*89G>A	NP_620148.1:n.*89G>A
XM_005257020.1:c.*89G>A	XP_005257077.1:n.*89G>A
XM_005257021.1:c.*89G>A	XP_005257078.1:n.*89G>A
XM_005257022.1:c.*89G>A	XP_005257079.1:n.*89G>A
XM_006721683.1:c.*89G>A	XP_006721746.1:n.*89G>A
XM_011524291.1:c.*89G>A	XP_011522593.1:n.*89G>A
XM_011524292.1:c.*89G>A	XP_011522594.1:n.*89G>A
XM_011524293.1:c.*89G>A	XP_011522595.1:n.*89G>A
XM_011524294.1:c.*89G>A	XP_011522596.1:n.*89G>A
XM_011524295.1:c.*89G>A	XP_011522597.1:n.*89G>A
XM_011524294.2:c.*89G>A	XP_011522596.1:n.*89G>A
XM_011524295.2:c.*89G>A	XP_011522597.1:n.*89G>A
XM_024450564.1:c.*89G>A	XP_024306332.1:n.*89G>A
XR_001752424.2:n.1739G>A
NM_001159773.2:c.*89G>A MANE Select	NP_001153245.1:n.*89G>A
NM_001159772.2:c.*89G>A	NP_001153244.1:n.*89G>A
NM_138793.4:c.*89G>A	NP_620148.1:n.*89G>A