Canonical Allele Identifier: CA2792557366

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915199_68915201del , CM000673.2:g.68915199_68915201del	GRCh38
NC_000011.9:g.68682667_68682669del , CM000673.1:g.68682667_68682669del	GRCh37
NC_000011.8:g.68439243_68439245del	NCBI36
NG_007976.1:g.16349_16351del , LRG_250:g.16349_16351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+176_912+178del MANE Select	ENSP00000255078.4:n.912+176_912+178del
ENST00000539224.2:c.1041+176_1041+178del
ENST00000674955.1:c.912+176_912+178del	ENSP00000502463.1:n.912+176_912+178del
ENST00000675118.1:c.259+176_259+178del
ENST00000675119.1:c.201+176_201+178del	ENSP00000501861.1:n.201+176_201+178del
ENST00000675305.1:c.201+176_201+178del	ENSP00000502365.1:n.201+176_201+178del
ENST00000675464.1:c.195+182_195+184del	ENSP00000502650.1:n.195+182_195+184del
ENST00000675615.1:c.912+176_912+178del	ENSP00000502413.1:n.912+176_912+178del
ENST00000675683.1:c.299+176_299+178del
ENST00000676173.1:n.956+176_956+178del
ENST00000676228.1:c.*235+176_*235+178del	ENSP00000502375.1:n.*235+176_*235+178del
ENST00000255078.7:c.912+176_912+178del	ENSP00000255078.3:n.912+176_912+178del
NM_002180.2:c.912+176_912+178del , LRG_250t1:c.912+176_912+178del	NP_002171.2:n.912+176_912+178del
XM_005273974.2:c.-100+176_-100+178del	XP_005274031.1:n.-100+176_-100+178del
XM_005273976.1:c.912+176_912+178del	XP_005274033.1:n.912+176_912+178del
XR_247198.1:n.1014+176_1014+178del
XR_949903.1:n.1014+176_1014+178del
XM_005273976.2:c.912+176_912+178del	XP_005274033.1:n.912+176_912+178del
XM_017017669.2:c.-100+176_-100+178del	XP_016873158.1:n.-100+176_-100+178del
XM_017017670.2:c.-100+176_-100+178del	XP_016873159.1:n.-100+176_-100+178del
XM_017017671.2:c.912+176_912+178del	XP_016873160.1:n.912+176_912+178del
XR_949903.3:n.1010+176_1010+178del
NM_002180.3:c.912+176_912+178del MANE Select	NP_002171.2:n.912+176_912+178del