Canonical Allele Identifier: CA2575348927

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815042_128815053del , CM000674.2:g.128815042_128815053del	GRCh38
NC_000012.11:g.129299587_129299598del , CM000674.1:g.129299587_129299598del	GRCh37
NC_000012.10:g.127865540_127865551del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.565_576del MANE Select	ENSP00000266771.5:p.Glu189_Arg192del
ENST00000266771.9:c.565_576del	ENSP00000266771.5:p.Glu189_Arg192del
ENST00000366292.6:n.877_888del
ENST00000376740.8:c.144_155del
ENST00000376744.8:c.401_412del
ENST00000535272.1:n.359_370del
ENST00000539703.1:n.215_226del
NM_145648.3:c.565_576del	NP_663623.1:p.Glu189_Arg192del
XM_011537895.1:c.715_726del	XP_011536197.1:p.Glu239_Arg242del
XR_429081.2:n.588_599del
XR_944494.1:n.738_749del
XR_944495.1:n.738_749del
XR_944496.1:n.738_749del
XR_944497.1:n.738_749del
XM_017018791.1:c.715_726del	XP_016874280.1:p.Glu239_Arg242del
XM_017018792.1:c.715_726del	XP_016874281.1:p.Glu239_Arg242del
XM_017018793.1:c.565_576del	XP_016874282.1:p.Glu189_Arg192del
XR_002957287.1:n.588_599del
XR_944496.2:n.738_749del
NM_145648.4:c.565_576del MANE Select	NP_663623.1:p.Glu189_Arg192del