Canonical Allele Identifier: CA354142041

Gene: SLC15A2

Linked Data

• dbSNP Id: rs1143671
• MyVariant Identifiers: chr3:g.121647286C>G (hg19) ; chr3:g.121928439C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000489711.6:c.1225C>G MANE Select	ENSP00000417085.1:p.Pro409Ala
ENST00000295605.6:c.1132C>G	ENSP00000295605.2:p.Pro378Ala
ENST00000465060.1:n.148C>G
ENST00000489711.5:c.1225C>G	ENSP00000417085.1:p.Pro409Ala
ENST00000489957.1:n.200C>G
NM_001145998.1:c.1132C>G	NP_001139470.1:p.Pro378Ala
NM_021082.3:c.1225C>G	NP_066568.3:p.Pro409Ala
XM_005247722.2:c.1225C>G	XP_005247779.1:p.Pro409Ala
XM_006713736.2:c.1225C>G	XP_006713799.1:p.Pro409Ala
XM_005247722.3:c.1225C>G	XP_005247779.1:p.Pro409Ala
XM_006713736.3:c.1225C>G	XP_006713799.1:p.Pro409Ala
XM_017007074.1:c.1225C>G	XP_016862563.1:p.Pro409Ala
NM_021082.4:c.1225C>G MANE Select	NP_066568.3:p.Pro409Ala
NM_001145998.2:c.1132C>G	NP_001139470.1:p.Pro378Ala