Canonical Allele Identifier: CA2071401616

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814712_128814713delinsGA , CM000674.2:g.128814712_128814713delinsGA	GRCh38
NC_000012.11:g.129299257_129299258delinsGA , CM000674.1:g.129299257_129299258delinsGA	GRCh37
NC_000012.10:g.127865210_127865211delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.842+62_842+63delinsTC MANE Select	ENSP00000266771.5:n.842+62_842+63delinsTC
ENST00000266771.9:c.842+62_842+63delinsTC	ENSP00000266771.5:n.842+62_842+63delinsTC
ENST00000366292.6:n.1154+62_1154+63delinsTC
ENST00000376740.8:c.421+62_421+63delinsTC
ENST00000376744.8:c.678+62_678+63delinsTC
ENST00000539703.1:n.492+62_492+63delinsTC
ENST00000614634.1:c.-1+62_-1+63delinsTC	ENSP00000483143.1:n.-1+62_-1+63delinsTC
NM_145648.3:c.842+62_842+63delinsTC	NP_663623.1:n.842+62_842+63delinsTC
XM_011537895.1:c.992+62_992+63delinsTC	XP_011536197.1:n.992+62_992+63delinsTC
XR_429081.2:n.865+62_865+63delinsTC
XR_944494.1:n.1015+62_1015+63delinsTC
XR_944495.1:n.1015+62_1015+63delinsTC
XR_944496.1:n.1015+62_1015+63delinsTC
XR_944497.1:n.1015+62_1015+63delinsTC
XM_017018791.1:c.992+62_992+63delinsTC	XP_016874280.1:n.992+62_992+63delinsTC
XM_017018792.1:c.992+62_992+63delinsTC	XP_016874281.1:n.992+62_992+63delinsTC
XM_017018793.1:c.842+62_842+63delinsTC	XP_016874282.1:n.842+62_842+63delinsTC
XR_002957287.1:n.865+62_865+63delinsTC
XR_944496.2:n.1015+62_1015+63delinsTC
NM_145648.4:c.842+62_842+63delinsTC MANE Select	NP_663623.1:n.842+62_842+63delinsTC