Canonical Allele Identifier: CA679620061

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1303774065
• MyVariant Identifiers: chr11:g.68675459_68675465del (hg19) ; chr11:g.68907991_68907997del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68907991_68907997del , CM000673.2:g.68907991_68907997del	GRCh38
NC_000011.9:g.68675459_68675465del , CM000673.1:g.68675459_68675465del	GRCh37
NC_000011.8:g.68432035_68432041del	NCBI36
NG_007976.1:g.9141_9147del , LRG_250:g.9141_9147del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.257-154_257-148del MANE Select	ENSP00000255078.4:n.257-154_257-148del
ENST00000539224.2:c.220-154_220-148del
ENST00000674583.1:c.220-154_220-148del
ENST00000674597.1:c.68-154_68-148del
ENST00000674955.1:c.257-154_257-148del	ENSP00000502463.1:n.257-154_257-148del
ENST00000675142.1:n.220-154_220-148del
ENST00000675469.1:c.133-154_133-148del
ENST00000675615.1:c.257-154_257-148del	ENSP00000502413.1:n.257-154_257-148del
ENST00000675674.1:n.220-154_220-148del
ENST00000675873.1:c.220-154_220-148del
ENST00000676173.1:n.301-154_301-148del
ENST00000676228.1:c.257-154_257-148del	ENSP00000502375.1:n.257-154_257-148del
ENST00000255078.7:c.257-154_257-148del	ENSP00000255078.3:n.257-154_257-148del
ENST00000539224.1:c.257-154_257-148del	ENSP00000440465.1:n.257-154_257-148del
ENST00000544541.1:c.87-154_87-148del	ENSP00000443343.1:n.87-154_87-148del
ENST00000545146.1:c.*127-154_*127-148del	ENSP00000456366.1:n.*127-154_*127-148del
NM_002180.2:c.257-154_257-148del , LRG_250t1:c.257-154_257-148del	NP_002171.2:n.257-154_257-148del
XM_005273974.2:c.-755-154_-755-148del	XP_005274031.1:n.-755-154_-755-148del
XM_005273976.1:c.257-154_257-148del	XP_005274033.1:n.257-154_257-148del
XR_247198.1:n.359-154_359-148del
XR_949903.1:n.359-154_359-148del
XM_005273976.2:c.257-154_257-148del	XP_005274033.1:n.257-154_257-148del
XM_017017669.2:c.-657-154_-657-148del	XP_016873158.1:n.-657-154_-657-148del
XM_017017671.2:c.257-154_257-148del	XP_016873160.1:n.257-154_257-148del
XR_949903.3:n.355-154_355-148del
NM_002180.3:c.257-154_257-148del MANE Select	NP_002171.2:n.257-154_257-148del