Canonical Allele Identifier: CA387234872

Gene: SLC15A4

Linked Data

• dbSNP Id: rs1364718992
• MyVariant Identifiers: chr12:g.129299363A>T (hg19) ; chr12:g.128814818A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814818A>T , CM000674.2:g.128814818A>T	GRCh38
NC_000012.11:g.129299363A>T , CM000674.1:g.129299363A>T	GRCh37
NC_000012.10:g.127865316A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.799T>A MANE Select	ENSP00000266771.5:p.Ser267Thr
ENST00000266771.9:c.799T>A	ENSP00000266771.5:p.Ser267Thr
ENST00000366292.6:n.1111T>A
ENST00000376740.8:c.378T>A
ENST00000376744.8:c.635T>A
ENST00000539703.1:n.449T>A
ENST00000614634.1:c.-44T>A	ENSP00000483143.1:n.-44T>A
NM_145648.3:c.799T>A	NP_663623.1:p.Ser267Thr
XM_011537895.1:c.949T>A	XP_011536197.1:p.Ser317Thr
XR_429081.2:n.822T>A
XR_944494.1:n.972T>A
XR_944495.1:n.972T>A
XR_944496.1:n.972T>A
XR_944497.1:n.972T>A
XM_017018791.1:c.949T>A	XP_016874280.1:p.Ser317Thr
XM_017018792.1:c.949T>A	XP_016874281.1:p.Ser317Thr
XM_017018793.1:c.799T>A	XP_016874282.1:p.Ser267Thr
XR_002957287.1:n.822T>A
XR_944496.2:n.972T>A
NM_145648.4:c.799T>A MANE Select	NP_663623.1:p.Ser267Thr