Canonical Allele Identifier: CA2071402205

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814998_128814999delinsTC , CM000674.2:g.128814998_128814999delinsTC	GRCh38
NC_000012.11:g.129299543_129299544delinsTC , CM000674.1:g.129299543_129299544delinsTC	GRCh37
NC_000012.10:g.127865496_127865497delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.618_619delinsGA MANE Select	ENSP00000266771.5:p.Ala206=
ENST00000266771.9:c.618_619delinsGA	ENSP00000266771.5:p.Ala206=
ENST00000366292.6:n.930_931delinsGA
ENST00000376740.8:c.197_198delinsGA
ENST00000376744.8:c.454_455delinsGA
ENST00000535272.1:n.412_413delinsGA
ENST00000539703.1:n.268_269delinsGA
NM_145648.3:c.618_619delinsGA	NP_663623.1:p.Ala206=
XM_011537895.1:c.768_769delinsGA	XP_011536197.1:p.Ala256=
XR_429081.2:n.641_642delinsGA
XR_944494.1:n.791_792delinsGA
XR_944495.1:n.791_792delinsGA
XR_944496.1:n.791_792delinsGA
XR_944497.1:n.791_792delinsGA
XM_017018791.1:c.768_769delinsGA	XP_016874280.1:p.Ala256=
XM_017018792.1:c.768_769delinsGA	XP_016874281.1:p.Ala256=
XM_017018793.1:c.618_619delinsGA	XP_016874282.1:p.Ala206=
XR_002957287.1:n.641_642delinsGA
XR_944496.2:n.791_792delinsGA
NM_145648.4:c.618_619delinsGA MANE Select	NP_663623.1:p.Ala206=