Canonical Allele Identifier: CA11453253

Gene: SLC15A2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121941817A>C , CM000665.2:g.121941817A>C	GRCh38
NC_000003.11:g.121660664A>C , CM000665.1:g.121660664A>C	GRCh37
NC_000003.10:g.123143354A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489711.6:c.*810A>C MANE Select	ENSP00000417085.1:n.*810A>C
ENST00000489711.5:c.*810A>C	ENSP00000417085.1:n.*810A>C
NM_001145998.1:c.*810A>C	NP_001139470.1:n.*810A>C
NM_021082.3:c.*810A>C	NP_066568.3:n.*810A>C
XM_005247722.2:c.*810A>C	XP_005247779.1:n.*810A>C
XM_005247722.3:c.*810A>C	XP_005247779.1:n.*810A>C
NM_021082.4:c.*810A>C MANE Select	NP_066568.3:n.*810A>C
NM_001145998.2:c.*810A>C	NP_001139470.1:n.*810A>C