Canonical Allele Identifier: CA2792557368

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915201_68915202del , CM000673.2:g.68915201_68915202del	GRCh38
NC_000011.9:g.68682669_68682670del , CM000673.1:g.68682669_68682670del	GRCh37
NC_000011.8:g.68439245_68439246del	NCBI36
NG_007976.1:g.16351_16352del , LRG_250:g.16351_16352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+178_912+179del MANE Select	ENSP00000255078.4:n.912+178_912+179del
ENST00000539224.2:c.1041+178_1041+179del
ENST00000674955.1:c.912+178_912+179del	ENSP00000502463.1:n.912+178_912+179del
ENST00000675118.1:c.259+178_259+179del
ENST00000675119.1:c.201+178_201+179del	ENSP00000501861.1:n.201+178_201+179del
ENST00000675305.1:c.201+178_201+179del	ENSP00000502365.1:n.201+178_201+179del
ENST00000675464.1:c.195+184_195+185del	ENSP00000502650.1:n.195+184_195+185del
ENST00000675615.1:c.912+178_912+179del	ENSP00000502413.1:n.912+178_912+179del
ENST00000675683.1:c.299+178_299+179del
ENST00000676173.1:n.956+178_956+179del
ENST00000676228.1:c.*235+178_*235+179del	ENSP00000502375.1:n.*235+178_*235+179del
ENST00000255078.7:c.912+178_912+179del	ENSP00000255078.3:n.912+178_912+179del
NM_002180.2:c.912+178_912+179del , LRG_250t1:c.912+178_912+179del	NP_002171.2:n.912+178_912+179del
XM_005273974.2:c.-100+178_-100+179del	XP_005274031.1:n.-100+178_-100+179del
XM_005273976.1:c.912+178_912+179del	XP_005274033.1:n.912+178_912+179del
XR_247198.1:n.1014+178_1014+179del
XR_949903.1:n.1014+178_1014+179del
XM_005273976.2:c.912+178_912+179del	XP_005274033.1:n.912+178_912+179del
XM_017017669.2:c.-100+178_-100+179del	XP_016873158.1:n.-100+178_-100+179del
XM_017017670.2:c.-100+178_-100+179del	XP_016873159.1:n.-100+178_-100+179del
XM_017017671.2:c.912+178_912+179del	XP_016873160.1:n.912+178_912+179del
XR_949903.3:n.1010+178_1010+179del
NM_002180.3:c.912+178_912+179del MANE Select	NP_002171.2:n.912+178_912+179del