Canonical Allele Identifier: CA1591132032

Gene: IRGM

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848349_150848352delinsGCCT , CM000667.2:g.150848349_150848352delinsGCCT	GRCh38
NC_000005.9:g.150227911_150227914delinsGCCT , CM000667.1:g.150227911_150227914delinsGCCT	GRCh37
NC_000005.8:g.150208104_150208107delinsGCCT	NCBI36
NG_027809.1:g.6827_6830delinsGCCT
NG_027809.2:g.6827_6830delinsGCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000522154.2:c.226_229delinsGCCT MANE Select	ENSP00000428220.1:p.Ala76=
ENST00000522154.1:c.226_229delinsGCCT	ENSP00000428220.1:p.Ala76=
NM_001145805.1:c.226_229delinsGCCT	NP_001139277.1:p.Ala76=
XM_011537641.1:c.226_229delinsGCCT	XP_011535943.1:p.Ala76=
NM_001346557.1:c.226_229delinsGCCT	NP_001333486.1:p.Ala76=
NM_001346557.2:c.226_229delinsGCCT	NP_001333486.1:p.Ala76=
NM_001145805.2:c.226_229delinsGCCT MANE Select	NP_001139277.1:p.Ala76=
NR_170598.1:n.1341_1344delinsGCCT