Canonical Allele Identifier: CA2621852413

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128814773-A-AAGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814773_128814774insAGAG , CM000674.2:g.128814773_128814774insAGAG	GRCh38
NC_000012.11:g.129299318_129299319insAGAG , CM000674.1:g.129299318_129299319insAGAG	GRCh37
NC_000012.10:g.127865271_127865272insAGAG	NCBI36

Transcript Alleles

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