Canonical Allele Identifier: CA563957468

Gene: IRGM

Linked Data

• dbSNP Id: rs1393929276
• gnomAD v2: 5-150227911-GCCT-G
• gnomAD v4: 5-150848349-GCCT-G
• MyVariant Identifiers: chr5:g.150227912_150227914del (hg19) ; chr5:g.150848350_150848352del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848353_150848355del , CM000667.2:g.150848353_150848355del	GRCh38
NC_000005.9:g.150227915_150227917del , CM000667.1:g.150227915_150227917del	GRCh37
NC_000005.8:g.150208108_150208110del	NCBI36
NG_027809.1:g.6831_6833del
NG_027809.2:g.6831_6833del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522154.2:c.230_232del MANE Select	ENSP00000428220.1:p.Ser77del
ENST00000522154.1:c.230_232del	ENSP00000428220.1:p.Ser77del
NM_001145805.1:c.230_232del	NP_001139277.1:p.Ser77del
XM_011537641.1:c.230_232del	XP_011535943.1:p.Ser77del
NM_001346557.1:c.230_232del	NP_001333486.1:p.Ser77del
NM_001346557.2:c.230_232del	NP_001333486.1:p.Ser77del
NM_001145805.2:c.230_232del MANE Select	NP_001139277.1:p.Ser77del
NR_170598.1:n.1345_1347del