Canonical Allele Identifier: CA2505867682

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815037del , CM000674.2:g.128815037del	GRCh38
NC_000012.11:g.129299582del , CM000674.1:g.129299582del	GRCh37
NC_000012.10:g.127865535del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.585del MANE Select	ENSP00000266771.5:p.Phe195LeufsTer16
ENST00000266771.9:c.585del	ENSP00000266771.5:p.Phe195LeufsTer16
ENST00000366292.6:n.897del
ENST00000376740.8:c.164del
ENST00000376744.8:c.421del
ENST00000535272.1:n.379del
ENST00000539703.1:n.235del
NM_145648.3:c.585del	NP_663623.1:p.Phe195LeufsTer16
XM_011537895.1:c.735del	XP_011536197.1:p.Phe245LeufsTer16
XR_429081.2:n.608del
XR_944494.1:n.758del
XR_944495.1:n.758del
XR_944496.1:n.758del
XR_944497.1:n.758del
XM_017018791.1:c.735del	XP_016874280.1:p.Phe245LeufsTer16
XM_017018792.1:c.735del	XP_016874281.1:p.Phe245LeufsTer16
XM_017018793.1:c.585del	XP_016874282.1:p.Phe195LeufsTer16
XR_002957287.1:n.608del
XR_944496.2:n.758del
NM_145648.4:c.585del MANE Select	NP_663623.1:p.Phe195LeufsTer16