Canonical Allele Identifier: CA354142036

Gene: SLC15A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121928439C>A , CM000665.2:g.121928439C>A	GRCh38
NC_000003.11:g.121647286C>A , CM000665.1:g.121647286C>A	GRCh37
NC_000003.10:g.123129976C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489711.6:c.1225C>A MANE Select	ENSP00000417085.1:p.Pro409Thr
ENST00000295605.6:c.1132C>A	ENSP00000295605.2:p.Pro378Thr
ENST00000465060.1:n.148C>A
ENST00000489711.5:c.1225C>A	ENSP00000417085.1:p.Pro409Thr
ENST00000489957.1:n.200C>A
NM_001145998.1:c.1132C>A	NP_001139470.1:p.Pro378Thr
NM_021082.3:c.1225C>A	NP_066568.3:p.Pro409Thr
XM_005247722.2:c.1225C>A	XP_005247779.1:p.Pro409Thr
XM_006713736.2:c.1225C>A	XP_006713799.1:p.Pro409Thr
XM_005247722.3:c.1225C>A	XP_005247779.1:p.Pro409Thr
XM_006713736.3:c.1225C>A	XP_006713799.1:p.Pro409Thr
XM_017007074.1:c.1225C>A	XP_016862563.1:p.Pro409Thr
NM_021082.4:c.1225C>A MANE Select	NP_066568.3:p.Pro409Thr
NM_001145998.2:c.1132C>A	NP_001139470.1:p.Pro378Thr