Canonical Allele Identifier: CA2614746211

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68915163-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915163_68915164insT , CM000673.2:g.68915163_68915164insT	GRCh38
NC_000011.9:g.68682631_68682632insT , CM000673.1:g.68682631_68682632insT	GRCh37
NC_000011.8:g.68439207_68439208insT	NCBI36
NG_007976.1:g.16313_16314insT , LRG_250:g.16313_16314insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+140_912+141insT MANE Select	ENSP00000255078.4:n.912+140_912+141insT
ENST00000539224.2:c.1041+140_1041+141insT
ENST00000674955.1:c.912+140_912+141insT	ENSP00000502463.1:n.912+140_912+141insT
ENST00000675118.1:c.259+140_259+141insT
ENST00000675119.1:c.201+140_201+141insT	ENSP00000501861.1:n.201+140_201+141insT
ENST00000675305.1:c.201+140_201+141insT	ENSP00000502365.1:n.201+140_201+141insT
ENST00000675464.1:c.195+146_195+147insT	ENSP00000502650.1:n.195+146_195+147insT
ENST00000675615.1:c.912+140_912+141insT	ENSP00000502413.1:n.912+140_912+141insT
ENST00000675683.1:c.299+140_299+141insT
ENST00000676173.1:n.956+140_956+141insT
ENST00000676228.1:c.*235+140_*235+141insT	ENSP00000502375.1:n.*235+140_*235+141insT
ENST00000255078.7:c.912+140_912+141insT	ENSP00000255078.3:n.912+140_912+141insT
NM_002180.2:c.912+140_912+141insT , LRG_250t1:c.912+140_912+141insT	NP_002171.2:n.912+140_912+141insT
XM_005273974.2:c.-100+140_-100+141insT	XP_005274031.1:n.-100+140_-100+141insT
XM_005273976.1:c.912+140_912+141insT	XP_005274033.1:n.912+140_912+141insT
XR_247198.1:n.1014+140_1014+141insT
XR_949903.1:n.1014+140_1014+141insT
XM_005273976.2:c.912+140_912+141insT	XP_005274033.1:n.912+140_912+141insT
XM_017017669.2:c.-100+140_-100+141insT	XP_016873158.1:n.-100+140_-100+141insT
XM_017017670.2:c.-100+140_-100+141insT	XP_016873159.1:n.-100+140_-100+141insT
XM_017017671.2:c.912+140_912+141insT	XP_016873160.1:n.912+140_912+141insT
XR_949903.3:n.1010+140_1010+141insT
NM_002180.3:c.912+140_912+141insT MANE Select	NP_002171.2:n.912+140_912+141insT