Canonical Allele Identifier: CA609576398

Gene: NUDT15

Linked Data

• dbSNP Id: rs1250912451
• gnomAD v2: 13-48619730-T-TA
• gnomAD v3: 13-48045594-T-TA
• gnomAD v4: 13-48045594-T-TA
• MyVariant Identifiers: chr13:g.48619730_48619731insA (hg19) ; chr13:g.48045594_48045595insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48045595dup , CM000675.2:g.48045595dup	GRCh38
NC_000013.10:g.48619731dup , CM000675.1:g.48619731dup	GRCh37
NC_000013.9:g.47517732dup	NCBI36
NG_047021.1:g.13029dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258662.3:c.356-65dup MANE Select	ENSP00000258662.1:n.356-65dup
ENST00000258662.2:c.356-65dup	ENSP00000258662.1:n.356-65dup
NM_018283.2:c.356-65dup	NP_060753.1:n.356-65dup
NM_018283.3:c.356-65dup	NP_060753.1:n.356-65dup
NR_136687.1:n.536-65dup
NR_136688.1:n.536-65dup
NM_018283.4:c.356-65dup MANE Select	NP_060753.1:n.356-65dup
NR_136687.2:n.377-65dup
NR_136688.2:n.377-65dup