Canonical Allele Identifier: CA939178395

Gene: IGHMBP2

Linked Data

• gnomAD v3: 11-68915166-C-CTGTTTTTTTTTT
• gnomAD v4: 11-68915166-C-CTGTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915167_68915168insGTTTTTTTTTTT , CM000673.2:g.68915167_68915168insGTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682635_68682636insGTTTTTTTTTTT , CM000673.1:g.68682635_68682636insGTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439211_68439212insGTTTTTTTTTTT	NCBI36
NG_007976.1:g.16317_16318insGTTTTTTTTTTT , LRG_250:g.16317_16318insGTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+144_912+145insGTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+144_912+145insGTTTTTTTTTTT
ENST00000539224.2:c.1041+144_1041+145insGTTTTTTTTTTT
ENST00000674955.1:c.912+144_912+145insGTTTTTTTTTTT	ENSP00000502463.1:n.912+144_912+145insGTTTTTTTTTTT
ENST00000675118.1:c.259+144_259+145insGTTTTTTTTTTT
ENST00000675119.1:c.201+144_201+145insGTTTTTTTTTTT	ENSP00000501861.1:n.201+144_201+145insGTTTTTTTTTTT
ENST00000675305.1:c.201+144_201+145insGTTTTTTTTTTT	ENSP00000502365.1:n.201+144_201+145insGTTTTTTTTTTT
ENST00000675464.1:c.195+150_195+151insGTTTTTTTTTTT	ENSP00000502650.1:n.195+150_195+151insGTTTTTTTTTTT
ENST00000675615.1:c.912+144_912+145insGTTTTTTTTTTT	ENSP00000502413.1:n.912+144_912+145insGTTTTTTTTTTT
ENST00000675683.1:c.299+144_299+145insGTTTTTTTTTTT
ENST00000676173.1:n.956+144_956+145insGTTTTTTTTTTT
ENST00000676228.1:c.*235+144_*235+145insGTTTTTTTTTTT	ENSP00000502375.1:n.*235+144_*235+145insGTTTTTTTTTTT
ENST00000255078.7:c.912+144_912+145insGTTTTTTTTTTT	ENSP00000255078.3:n.912+144_912+145insGTTTTTTTTTTT
NM_002180.2:c.912+144_912+145insGTTTTTTTTTTT , LRG_250t1:c.912+144_912+145insGTTTTTTTTTTT	NP_002171.2:n.912+144_912+145insGTTTTTTTTTTT
XM_005273974.2:c.-100+144_-100+145insGTTTTTTTTTTT	XP_005274031.1:n.-100+144_-100+145insGTTTTTTTTTTT
XM_005273976.1:c.912+144_912+145insGTTTTTTTTTTT	XP_005274033.1:n.912+144_912+145insGTTTTTTTTTTT
XR_247198.1:n.1014+144_1014+145insGTTTTTTTTTTT
XR_949903.1:n.1014+144_1014+145insGTTTTTTTTTTT
XM_005273976.2:c.912+144_912+145insGTTTTTTTTTTT	XP_005274033.1:n.912+144_912+145insGTTTTTTTTTTT
XM_017017669.2:c.-100+144_-100+145insGTTTTTTTTTTT	XP_016873158.1:n.-100+144_-100+145insGTTTTTTTTTTT
XM_017017670.2:c.-100+144_-100+145insGTTTTTTTTTTT	XP_016873159.1:n.-100+144_-100+145insGTTTTTTTTTTT
XM_017017671.2:c.912+144_912+145insGTTTTTTTTTTT	XP_016873160.1:n.912+144_912+145insGTTTTTTTTTTT
XR_949903.3:n.1010+144_1010+145insGTTTTTTTTTTT
NM_002180.3:c.912+144_912+145insGTTTTTTTTTTT MANE Select	NP_002171.2:n.912+144_912+145insGTTTTTTTTTTT