Canonical Allele Identifier: CA2621852147

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128814485-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814488del , CM000674.2:g.128814488del	GRCh38
NC_000012.11:g.129299033del , CM000674.1:g.129299033del	GRCh37
NC_000012.10:g.127864986del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.842+289del MANE Select	ENSP00000266771.5:n.842+289del
ENST00000266771.9:c.842+289del	ENSP00000266771.5:n.842+289del
ENST00000366292.6:n.1154+289del
ENST00000376740.8:c.421+289del
ENST00000376744.8:c.678+289del
ENST00000539703.1:n.492+289del
ENST00000614634.1:c.-1+289del	ENSP00000483143.1:n.-1+289del
NM_145648.3:c.842+289del	NP_663623.1:n.842+289del
XM_011537895.1:c.992+289del	XP_011536197.1:n.992+289del
XR_429081.2:n.865+289del
XR_944494.1:n.1015+289del
XR_944495.1:n.1015+289del
XR_944496.1:n.1015+289del
XR_944497.1:n.1015+289del
XM_017018791.1:c.992+289del	XP_016874280.1:n.992+289del
XM_017018792.1:c.992+289del	XP_016874281.1:n.992+289del
XM_017018793.1:c.842+289del	XP_016874282.1:n.842+289del
XR_002957287.1:n.865+289del
XR_944496.2:n.1015+289del
NM_145648.4:c.842+289del MANE Select	NP_663623.1:n.842+289del