Canonical Allele Identifier: CA2621852412

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128814767-GTGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814769_128814772del , CM000674.2:g.128814769_128814772del	GRCh38
NC_000012.11:g.129299314_129299317del , CM000674.1:g.129299314_129299317del	GRCh37
NC_000012.10:g.127865267_127865270del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266771.10:c.842+4_842+7del MANE Select	ENSP00000266771.5:n.842+4_842+7del
ENST00000266771.9:c.842+4_842+7del	ENSP00000266771.5:n.842+4_842+7del
ENST00000366292.6:n.1154+4_1154+7del
ENST00000376740.8:c.421+4_421+7del
ENST00000376744.8:c.678+4_678+7del
ENST00000539703.1:n.492+4_492+7del
ENST00000614634.1:c.-1+4_-1+7del	ENSP00000483143.1:n.-1+4_-1+7del
NM_145648.3:c.842+4_842+7del	NP_663623.1:n.842+4_842+7del
XM_011537895.1:c.992+4_992+7del	XP_011536197.1:n.992+4_992+7del
XR_429081.2:n.865+4_865+7del
XR_944494.1:n.1015+4_1015+7del
XR_944495.1:n.1015+4_1015+7del
XR_944496.1:n.1015+4_1015+7del
XR_944497.1:n.1015+4_1015+7del
XM_017018791.1:c.992+4_992+7del	XP_016874280.1:n.992+4_992+7del
XM_017018792.1:c.992+4_992+7del	XP_016874281.1:n.992+4_992+7del
XM_017018793.1:c.842+4_842+7del	XP_016874282.1:n.842+4_842+7del
XR_002957287.1:n.865+4_865+7del
XR_944496.2:n.1015+4_1015+7del
NM_145648.4:c.842+4_842+7del MANE Select	NP_663623.1:n.842+4_842+7del