Canonical Allele Identifier: CA939172667

Gene: IGHMBP2

Linked Data

• gnomAD v3: 11-68908015-A-ATTT
• gnomAD v4: 11-68908015-A-ATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908015_68908016insTTT , CM000673.2:g.68908015_68908016insTTT	GRCh38
NC_000011.9:g.68675483_68675484insTTT , CM000673.1:g.68675483_68675484insTTT	GRCh37
NC_000011.8:g.68432059_68432060insTTT	NCBI36
NG_007976.1:g.9165_9166insTTT , LRG_250:g.9165_9166insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.257-130_257-129insTTT MANE Select	ENSP00000255078.4:n.257-130_257-129insTTT
ENST00000539224.2:c.220-130_220-129insTTT
ENST00000674583.1:c.220-130_220-129insTTT
ENST00000674597.1:c.68-130_68-129insTTT
ENST00000674955.1:c.257-130_257-129insTTT	ENSP00000502463.1:n.257-130_257-129insTTT
ENST00000675142.1:n.220-130_220-129insTTT
ENST00000675469.1:c.133-130_133-129insTTT
ENST00000675615.1:c.257-130_257-129insTTT	ENSP00000502413.1:n.257-130_257-129insTTT
ENST00000675674.1:n.220-130_220-129insTTT
ENST00000675873.1:c.220-130_220-129insTTT
ENST00000676173.1:n.301-130_301-129insTTT
ENST00000676228.1:c.257-130_257-129insTTT	ENSP00000502375.1:n.257-130_257-129insTTT
ENST00000255078.7:c.257-130_257-129insTTT	ENSP00000255078.3:n.257-130_257-129insTTT
ENST00000539224.1:c.257-130_257-129insTTT	ENSP00000440465.1:n.257-130_257-129insTTT
ENST00000544541.1:c.87-130_87-129insTTT	ENSP00000443343.1:n.87-130_87-129insTTT
ENST00000545146.1:c.*127-130_*127-129insTTT	ENSP00000456366.1:n.*127-130_*127-129insTTT
NM_002180.2:c.257-130_257-129insTTT , LRG_250t1:c.257-130_257-129insTTT	NP_002171.2:n.257-130_257-129insTTT
XM_005273974.2:c.-755-130_-755-129insTTT	XP_005274031.1:n.-755-130_-755-129insTTT
XM_005273976.1:c.257-130_257-129insTTT	XP_005274033.1:n.257-130_257-129insTTT
XR_247198.1:n.359-130_359-129insTTT
XR_949903.1:n.359-130_359-129insTTT
XM_005273976.2:c.257-130_257-129insTTT	XP_005274033.1:n.257-130_257-129insTTT
XM_017017669.2:c.-657-130_-657-129insTTT	XP_016873158.1:n.-657-130_-657-129insTTT
XM_017017671.2:c.257-130_257-129insTTT	XP_016873160.1:n.257-130_257-129insTTT
XR_949903.3:n.355-130_355-129insTTT
NM_002180.3:c.257-130_257-129insTTT MANE Select	NP_002171.2:n.257-130_257-129insTTT