Canonical Allele Identifier: CA388154554

Gene: NUDT15

Linked Data

• MyVariant Identifiers: chr13:g.48619924A>T (hg19) ; chr13:g.48045788A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48045788A>T , CM000675.2:g.48045788A>T	GRCh38
NC_000013.10:g.48619924A>T , CM000675.1:g.48619924A>T	GRCh37
NC_000013.9:g.47517925A>T	NCBI36
NG_047021.1:g.13222A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258662.3:c.484A>T MANE Select	ENSP00000258662.1:p.Asn162Tyr
ENST00000258662.2:c.484A>T	ENSP00000258662.1:p.Asn162Tyr
NM_018283.2:c.484A>T	NP_060753.1:p.Asn162Tyr
NM_018283.3:c.484A>T	NP_060753.1:p.Asn162Tyr
NR_136687.1:n.664A>T
NR_136688.1:n.664A>T
NM_018283.4:c.484A>T MANE Select	NP_060753.1:p.Asn162Tyr
NR_136687.2:n.505A>T
NR_136688.2:n.505A>T