Canonical Allele Identifier: CA1591131979

Gene: IRGM

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848247T= , CM000667.2:g.150848247T=	GRCh38
NC_000005.9:g.150227809T= , CM000667.1:g.150227809T=	GRCh37
NC_000005.8:g.150208002T=	NCBI36
NG_027809.1:g.6725T=
NG_027809.2:g.6725T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522154.2:c.124T= MANE Select	ENSP00000428220.1:p.Ser42=
ENST00000522154.1:c.124T=	ENSP00000428220.1:p.Ser42=
NM_001145805.1:c.124T=	NP_001139277.1:p.Ser42=
XM_011537641.1:c.124T=	XP_011535943.1:p.Ser42=
NM_001346557.1:c.124T=	NP_001333486.1:p.Ser42=
NM_001346557.2:c.124T=	NP_001333486.1:p.Ser42=
NM_001145805.2:c.124T= MANE Select	NP_001139277.1:p.Ser42=
NR_170598.1:n.1239T=