Canonical Allele Identifier: CA387235599

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128815057-C-T
• MyVariant Identifiers: chr12:g.129299602C>T (hg19) ; chr12:g.128815057C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815057C>T , CM000674.2:g.128815057C>T	GRCh38
NC_000012.11:g.129299602C>T , CM000674.1:g.129299602C>T	GRCh37
NC_000012.10:g.127865555C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.560G>A MANE Select	ENSP00000266771.5:p.Gly187Asp
ENST00000266771.9:c.560G>A	ENSP00000266771.5:p.Gly187Asp
ENST00000366292.6:n.872G>A
ENST00000376740.8:c.139G>A
ENST00000376744.8:c.396G>A
ENST00000535272.1:n.354G>A
ENST00000539703.1:n.210G>A
NM_145648.3:c.560G>A	NP_663623.1:p.Gly187Asp
XM_011537895.1:c.710G>A	XP_011536197.1:p.Gly237Asp
XR_429081.2:n.583G>A
XR_944494.1:n.733G>A
XR_944495.1:n.733G>A
XR_944496.1:n.733G>A
XR_944497.1:n.733G>A
XM_017018791.1:c.710G>A	XP_016874280.1:p.Gly237Asp
XM_017018792.1:c.710G>A	XP_016874281.1:p.Gly237Asp
XM_017018793.1:c.560G>A	XP_016874282.1:p.Gly187Asp
XR_002957287.1:n.583G>A
XR_944496.2:n.733G>A
NM_145648.4:c.560G>A MANE Select	NP_663623.1:p.Gly187Asp