Canonical Allele Identifier: CA2071402258

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815021_128815022delinsTA , CM000674.2:g.128815021_128815022delinsTA	GRCh38
NC_000012.11:g.129299566_129299567delinsTA , CM000674.1:g.129299566_129299567delinsTA	GRCh37
NC_000012.10:g.127865519_127865520delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.595_596delinsTA MANE Select	ENSP00000266771.5:p.Tyr199=
ENST00000266771.9:c.595_596delinsTA	ENSP00000266771.5:p.Tyr199=
ENST00000366292.6:n.907_908delinsTA
ENST00000376740.8:c.174_175delinsTA
ENST00000376744.8:c.431_432delinsTA
ENST00000535272.1:n.389_390delinsTA
ENST00000539703.1:n.245_246delinsTA
NM_145648.3:c.595_596delinsTA	NP_663623.1:p.Tyr199=
XM_011537895.1:c.745_746delinsTA	XP_011536197.1:p.Tyr249=
XR_429081.2:n.618_619delinsTA
XR_944494.1:n.768_769delinsTA
XR_944495.1:n.768_769delinsTA
XR_944496.1:n.768_769delinsTA
XR_944497.1:n.768_769delinsTA
XM_017018791.1:c.745_746delinsTA	XP_016874280.1:p.Tyr249=
XM_017018792.1:c.745_746delinsTA	XP_016874281.1:p.Tyr249=
XM_017018793.1:c.595_596delinsTA	XP_016874282.1:p.Tyr199=
XR_002957287.1:n.618_619delinsTA
XR_944496.2:n.768_769delinsTA
NM_145648.4:c.595_596delinsTA MANE Select	NP_663623.1:p.Tyr199=