Canonical Allele Identifier: CA679620101

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1351064031
• MyVariant Identifiers: chr11:g.68675517_68675522del (hg19) ; chr11:g.68908049_68908054del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908052_68908057del , CM000673.2:g.68908052_68908057del	GRCh38
NC_000011.9:g.68675520_68675525del , CM000673.1:g.68675520_68675525del	GRCh37
NC_000011.8:g.68432096_68432101del	NCBI36
NG_007976.1:g.9202_9207del , LRG_250:g.9202_9207del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.257-93_257-88del MANE Select	ENSP00000255078.4:n.257-93_257-88del
ENST00000539224.2:c.220-93_220-88del
ENST00000674583.1:c.220-93_220-88del
ENST00000674597.1:c.68-93_68-88del
ENST00000674955.1:c.257-93_257-88del	ENSP00000502463.1:n.257-93_257-88del
ENST00000675142.1:n.220-93_220-88del
ENST00000675469.1:c.133-93_133-88del
ENST00000675615.1:c.257-93_257-88del	ENSP00000502413.1:n.257-93_257-88del
ENST00000675674.1:n.220-93_220-88del
ENST00000675873.1:c.220-93_220-88del
ENST00000676173.1:n.301-93_301-88del
ENST00000676228.1:c.257-93_257-88del	ENSP00000502375.1:n.257-93_257-88del
ENST00000255078.7:c.257-93_257-88del	ENSP00000255078.3:n.257-93_257-88del
ENST00000539224.1:c.257-93_257-88del	ENSP00000440465.1:n.257-93_257-88del
ENST00000544541.1:c.87-93_87-88del	ENSP00000443343.1:n.87-93_87-88del
ENST00000545146.1:c.*127-93_*127-88del	ENSP00000456366.1:n.*127-93_*127-88del
NM_002180.2:c.257-93_257-88del , LRG_250t1:c.257-93_257-88del	NP_002171.2:n.257-93_257-88del
XM_005273974.2:c.-755-93_-755-88del	XP_005274031.1:n.-755-93_-755-88del
XM_005273976.1:c.257-93_257-88del	XP_005274033.1:n.257-93_257-88del
XR_247198.1:n.359-93_359-88del
XR_949903.1:n.359-93_359-88del
XM_005273976.2:c.257-93_257-88del	XP_005274033.1:n.257-93_257-88del
XM_017017669.2:c.-657-93_-657-88del	XP_016873158.1:n.-657-93_-657-88del
XM_017017671.2:c.257-93_257-88del	XP_016873160.1:n.257-93_257-88del
XR_949903.3:n.355-93_355-88del
NM_002180.3:c.257-93_257-88del MANE Select	NP_002171.2:n.257-93_257-88del