Canonical Allele Identifier: CA2621852416

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128814871-G-GTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814875_128814877dup , CM000674.2:g.128814875_128814877dup	GRCh38
NC_000012.11:g.129299420_129299422dup , CM000674.1:g.129299420_129299422dup	GRCh37
NC_000012.10:g.127865373_127865375dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.743_745dup MANE Select	ENSP00000266771.5:p.Ile248_Thr249insIle
ENST00000266771.9:c.743_745dup	ENSP00000266771.5:p.Ile248_Thr249insIle
ENST00000366292.6:n.1055_1057dup
ENST00000376740.8:c.322_324dup
ENST00000376744.8:c.579_581dup
ENST00000539703.1:n.393_395dup
ENST00000614634.1:c.-100_-98dup	ENSP00000483143.1:n.-100_-98dup
NM_145648.3:c.743_745dup	NP_663623.1:p.Ile248_Thr249insIle
XM_011537895.1:c.893_895dup	XP_011536197.1:p.Ile298_Thr299insIle
XR_429081.2:n.766_768dup
XR_944494.1:n.916_918dup
XR_944495.1:n.916_918dup
XR_944496.1:n.916_918dup
XR_944497.1:n.916_918dup
XM_017018791.1:c.893_895dup	XP_016874280.1:p.Ile298_Thr299insIle
XM_017018792.1:c.893_895dup	XP_016874281.1:p.Ile298_Thr299insIle
XM_017018793.1:c.743_745dup	XP_016874282.1:p.Ile248_Thr249insIle
XR_002957287.1:n.766_768dup
XR_944496.2:n.916_918dup
NM_145648.4:c.743_745dup MANE Select	NP_663623.1:p.Ile248_Thr249insIle