Canonical Allele Identifier: CA2837832567

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915176_68915177insC , CM000673.2:g.68915176_68915177insC	GRCh38
NC_000011.9:g.68682644_68682645insC , CM000673.1:g.68682644_68682645insC	GRCh37
NC_000011.8:g.68439220_68439221insC	NCBI36
NG_007976.1:g.16326_16327insC , LRG_250:g.16326_16327insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+153_912+154insC MANE Select	ENSP00000255078.4:n.912+153_912+154insC
ENST00000539224.2:c.1041+153_1041+154insC
ENST00000674955.1:c.912+153_912+154insC	ENSP00000502463.1:n.912+153_912+154insC
ENST00000675118.1:c.259+153_259+154insC
ENST00000675119.1:c.201+153_201+154insC	ENSP00000501861.1:n.201+153_201+154insC
ENST00000675305.1:c.201+153_201+154insC	ENSP00000502365.1:n.201+153_201+154insC
ENST00000675464.1:c.195+159_195+160insC	ENSP00000502650.1:n.195+159_195+160insC
ENST00000675615.1:c.912+153_912+154insC	ENSP00000502413.1:n.912+153_912+154insC
ENST00000675683.1:c.299+153_299+154insC
ENST00000676173.1:n.956+153_956+154insC
ENST00000676228.1:c.*235+153_*235+154insC	ENSP00000502375.1:n.*235+153_*235+154insC
ENST00000255078.7:c.912+153_912+154insC	ENSP00000255078.3:n.912+153_912+154insC
NM_002180.2:c.912+153_912+154insC , LRG_250t1:c.912+153_912+154insC	NP_002171.2:n.912+153_912+154insC
XM_005273974.2:c.-100+153_-100+154insC	XP_005274031.1:n.-100+153_-100+154insC
XM_005273976.1:c.912+153_912+154insC	XP_005274033.1:n.912+153_912+154insC
XR_247198.1:n.1014+153_1014+154insC
XR_949903.1:n.1014+153_1014+154insC
XM_005273976.2:c.912+153_912+154insC	XP_005274033.1:n.912+153_912+154insC
XM_017017669.2:c.-100+153_-100+154insC	XP_016873158.1:n.-100+153_-100+154insC
XM_017017670.2:c.-100+153_-100+154insC	XP_016873159.1:n.-100+153_-100+154insC
XM_017017671.2:c.912+153_912+154insC	XP_016873160.1:n.912+153_912+154insC
XR_949903.3:n.1010+153_1010+154insC
NM_002180.3:c.912+153_912+154insC MANE Select	NP_002171.2:n.912+153_912+154insC