Canonical Allele Identifier: CA698626283

Gene: NUDT15

Linked Data

• dbSNP Id: rs1237767634
• MyVariant Identifiers: chr13:g.48619848_48619849insGCTGGTCCAGCTTTTCT (hg19) ; chr13:g.48045712_48045713insGCTGGTCCAGCTTTTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48045713_48045714insCTGGTCCAGCTTTTCTG , CM000675.2:g.48045713_48045714insCTGGTCCAGCTTTTCTG	GRCh38
NC_000013.10:g.48619849_48619850insCTGGTCCAGCTTTTCTG , CM000675.1:g.48619849_48619850insCTGGTCCAGCTTTTCTG	GRCh37
NC_000013.9:g.47517850_47517851insCTGGTCCAGCTTTTCTG	NCBI36
NG_047021.1:g.13147_13148insCTGGTCCAGCTTTTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258662.3:c.409_410insCTGGTCCAGCTTTTCTG MANE Select	ENSP00000258662.1:p.Gly137AlafsTer11
ENST00000258662.2:c.409_410insCTGGTCCAGCTTTTCTG	ENSP00000258662.1:p.Gly137AlafsTer11
NM_018283.2:c.409_410insCTGGTCCAGCTTTTCTG	NP_060753.1:p.Gly137AlafsTer11
NM_018283.3:c.409_410insCTGGTCCAGCTTTTCTG	NP_060753.1:p.Gly137AlafsTer11
NR_136687.1:n.589_590insCTGGTCCAGCTTTTCTG
NR_136688.1:n.589_590insCTGGTCCAGCTTTTCTG
NM_018283.4:c.409_410insCTGGTCCAGCTTTTCTG MANE Select	NP_060753.1:p.Gly137AlafsTer11
NR_136687.2:n.430_431insCTGGTCCAGCTTTTCTG
NR_136688.2:n.430_431insCTGGTCCAGCTTTTCTG