Canonical Allele Identifier: CA939178339

Gene: IGHMBP2

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915177_68915178insATTTTTTTTTTTTTTTT , CM000673.2:g.68915177_68915178insATTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682645_68682646insATTTTTTTTTTTTTTTT , CM000673.1:g.68682645_68682646insATTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439221_68439222insATTTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.16327_16328insATTTTTTTTTTTTTTTT , LRG_250:g.16327_16328insATTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+154_912+155insATTTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+154_912+155insATTTTTTTTTTTTTTTT
ENST00000539224.2:c.1041+154_1041+155insATTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+154_912+155insATTTTTTTTTTTTTTTT	ENSP00000502463.1:n.912+154_912+155insATTTTTTTTTTTTTTTT
ENST00000675118.1:c.259+154_259+155insATTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+154_201+155insATTTTTTTTTTTTTTTT	ENSP00000501861.1:n.201+154_201+155insATTTTTTTTTTTTTTTT
ENST00000675305.1:c.201+154_201+155insATTTTTTTTTTTTTTTT	ENSP00000502365.1:n.201+154_201+155insATTTTTTTTTTTTTTTT
ENST00000675464.1:c.195+160_195+161insATTTTTTTTTTTTTTTT	ENSP00000502650.1:n.195+160_195+161insATTTTTTTTTTTTTTTT
ENST00000675615.1:c.912+154_912+155insATTTTTTTTTTTTTTTT	ENSP00000502413.1:n.912+154_912+155insATTTTTTTTTTTTTTTT
ENST00000675683.1:c.299+154_299+155insATTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+154_956+155insATTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+154_*235+155insATTTTTTTTTTTTTTTT	ENSP00000502375.1:n.*235+154_*235+155insATTTTTTTTTTTTTTTT
ENST00000255078.7:c.912+154_912+155insATTTTTTTTTTTTTTTT	ENSP00000255078.3:n.912+154_912+155insATTTTTTTTTTTTTTTT
NM_002180.2:c.912+154_912+155insATTTTTTTTTTTTTTTT , LRG_250t1:c.912+154_912+155insATTTTTTTTTTTTTTTT	NP_002171.2:n.912+154_912+155insATTTTTTTTTTTTTTTT
XM_005273974.2:c.-100+154_-100+155insATTTTTTTTTTTTTTTT	XP_005274031.1:n.-100+154_-100+155insATTTTTTTTTTTTTTTT
XM_005273976.1:c.912+154_912+155insATTTTTTTTTTTTTTTT	XP_005274033.1:n.912+154_912+155insATTTTTTTTTTTTTTTT
XR_247198.1:n.1014+154_1014+155insATTTTTTTTTTTTTTTT
XR_949903.1:n.1014+154_1014+155insATTTTTTTTTTTTTTTT
XM_005273976.2:c.912+154_912+155insATTTTTTTTTTTTTTTT	XP_005274033.1:n.912+154_912+155insATTTTTTTTTTTTTTTT
XM_017017669.2:c.-100+154_-100+155insATTTTTTTTTTTTTTTT	XP_016873158.1:n.-100+154_-100+155insATTTTTTTTTTTTTTTT
XM_017017670.2:c.-100+154_-100+155insATTTTTTTTTTTTTTTT	XP_016873159.1:n.-100+154_-100+155insATTTTTTTTTTTTTTTT
XM_017017671.2:c.912+154_912+155insATTTTTTTTTTTTTTTT	XP_016873160.1:n.912+154_912+155insATTTTTTTTTTTTTTTT
XR_949903.3:n.1010+154_1010+155insATTTTTTTTTTTTTTTT
NM_002180.3:c.912+154_912+155insATTTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.912+154_912+155insATTTTTTTTTTTTTTTT