Canonical Allele Identifier: CA15073548

Gene: NT5C1A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39667123T>G , CM000663.2:g.39667123T>G	GRCh38
NC_000001.10:g.40132795T>G , CM000663.1:g.40132795T>G	GRCh37
NC_000001.9:g.39905382T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235628.2:c.136-887A>C MANE Select	ENSP00000235628.1:n.136-887A>C
ENST00000235628.1:c.136-887A>C	ENSP00000235628.1:n.136-887A>C
NM_032526.2:c.136-887A>C	NP_115915.1:n.136-887A>C
NM_032526.3:c.136-887A>C MANE Select	NP_115915.1:n.136-887A>C