Canonical Allele Identifier: CA387235335

Gene: SLC15A4

Linked Data

• MyVariant Identifiers: chr12:g.129299483C>T (hg19) ; chr12:g.128814938C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814938C>T , CM000674.2:g.128814938C>T	GRCh38
NC_000012.11:g.129299483C>T , CM000674.1:g.129299483C>T	GRCh37
NC_000012.10:g.127865436C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.679G>A MANE Select	ENSP00000266771.5:p.Ala227Thr
ENST00000266771.9:c.679G>A	ENSP00000266771.5:p.Ala227Thr
ENST00000366292.6:n.991G>A
ENST00000376740.8:c.258G>A
ENST00000376744.8:c.515G>A
ENST00000539703.1:n.329G>A
ENST00000614634.1:c.-164G>A	ENSP00000483143.1:n.-164G>A
NM_145648.3:c.679G>A	NP_663623.1:p.Ala227Thr
XM_011537895.1:c.829G>A	XP_011536197.1:p.Ala277Thr
XR_429081.2:n.702G>A
XR_944494.1:n.852G>A
XR_944495.1:n.852G>A
XR_944496.1:n.852G>A
XR_944497.1:n.852G>A
XM_017018791.1:c.829G>A	XP_016874280.1:p.Ala277Thr
XM_017018792.1:c.829G>A	XP_016874281.1:p.Ala277Thr
XM_017018793.1:c.679G>A	XP_016874282.1:p.Ala227Thr
XR_002957287.1:n.702G>A
XR_944496.2:n.852G>A
NM_145648.4:c.679G>A MANE Select	NP_663623.1:p.Ala227Thr