Canonical Allele Identifier: CA2071401859

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814815_128814816delinsAG , CM000674.2:g.128814815_128814816delinsAG	GRCh38
NC_000012.11:g.129299360_129299361delinsAG , CM000674.1:g.129299360_129299361delinsAG	GRCh37
NC_000012.10:g.127865313_127865314delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.801_802delinsCT MANE Select	ENSP00000266771.5:p.Ser267=
ENST00000266771.9:c.801_802delinsCT	ENSP00000266771.5:p.Ser267=
ENST00000366292.6:n.1113_1114delinsCT
ENST00000376740.8:c.380_381delinsCT
ENST00000376744.8:c.637_638delinsCT
ENST00000539703.1:n.451_452delinsCT
ENST00000614634.1:c.-42_-41delinsCT	ENSP00000483143.1:n.-42_-41delinsCT
NM_145648.3:c.801_802delinsCT	NP_663623.1:p.Ser267=
XM_011537895.1:c.951_952delinsCT	XP_011536197.1:p.Ser317=
XR_429081.2:n.824_825delinsCT
XR_944494.1:n.974_975delinsCT
XR_944495.1:n.974_975delinsCT
XR_944496.1:n.974_975delinsCT
XR_944497.1:n.974_975delinsCT
XM_017018791.1:c.951_952delinsCT	XP_016874280.1:p.Ser317=
XM_017018792.1:c.951_952delinsCT	XP_016874281.1:p.Ser317=
XM_017018793.1:c.801_802delinsCT	XP_016874282.1:p.Ser267=
XR_002957287.1:n.824_825delinsCT
XR_944496.2:n.974_975delinsCT
NM_145648.4:c.801_802delinsCT MANE Select	NP_663623.1:p.Ser267=