Canonical Allele Identifier: CA1591131976

Gene: IRGM

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848244G= , CM000667.2:g.150848244G=	GRCh38
NC_000005.9:g.150227806G= , CM000667.1:g.150227806G=	GRCh37
NC_000005.8:g.150207999G=	NCBI36
NG_027809.1:g.6722G=
NG_027809.2:g.6722G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522154.2:c.121G= MANE Select	ENSP00000428220.1:p.Asp41=
ENST00000522154.1:c.121G=	ENSP00000428220.1:p.Asp41=
NM_001145805.1:c.121G=	NP_001139277.1:p.Asp41=
XM_011537641.1:c.121G=	XP_011535943.1:p.Asp41=
NM_001346557.1:c.121G=	NP_001333486.1:p.Asp41=
NM_001346557.2:c.121G=	NP_001333486.1:p.Asp41=
NM_001145805.2:c.121G= MANE Select	NP_001139277.1:p.Asp41=
NR_170598.1:n.1236G=