Canonical Allele Identifier: CA387235079

Gene: SLC15A4

Linked Data

• MyVariant Identifiers: chr12:g.128814862del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814863del , CM000674.2:g.128814863del	GRCh38
NC_000012.11:g.129299408del , CM000674.1:g.129299408del	GRCh37
NC_000012.10:g.127865361del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.755del MANE Select	ENSP00000266771.5:p.Pro252LeufsTer13
ENST00000266771.9:c.755del	ENSP00000266771.5:p.Pro252LeufsTer13
ENST00000366292.6:n.1067del
ENST00000376740.8:c.334del
ENST00000376744.8:c.591del
ENST00000539703.1:n.405del
ENST00000614634.1:c.-88del	ENSP00000483143.1:n.-88del
NM_145648.3:c.755del	NP_663623.1:p.Pro252LeufsTer13
XM_011537895.1:c.905del	XP_011536197.1:p.Pro302LeufsTer13
XR_429081.2:n.778del
XR_944494.1:n.928del
XR_944495.1:n.928del
XR_944496.1:n.928del
XR_944497.1:n.928del
XM_017018791.1:c.905del	XP_016874280.1:p.Pro302LeufsTer13
XM_017018792.1:c.905del	XP_016874281.1:p.Pro302LeufsTer13
XM_017018793.1:c.755del	XP_016874282.1:p.Pro252LeufsTer13
XR_002957287.1:n.778del
XR_944496.2:n.928del
NM_145648.4:c.755del MANE Select	NP_663623.1:p.Pro252LeufsTer13