Canonical Allele Identifier: CA2614746161
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68908059del , CM000673.2:g.68908059del GRCh38
NC_000011.9:g.68675527del , CM000673.1:g.68675527del GRCh37
NC_000011.8:g.68432103del NCBI36
NG_007976.1:g.9209del , LRG_250:g.9209del

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.257-86del MANE Select ENSP00000255078.4:n.257-86del
ENST00000539224.2:c.220-86del
ENST00000674583.1:c.220-86del
ENST00000674597.1:c.68-86del
ENST00000674955.1:c.257-86del ENSP00000502463.1:n.257-86del
ENST00000675142.1:n.220-86del
ENST00000675469.1:c.133-86del
ENST00000675615.1:c.257-86del ENSP00000502413.1:n.257-86del
ENST00000675674.1:n.220-86del
ENST00000675873.1:c.220-86del
ENST00000676173.1:n.301-86del
ENST00000676228.1:c.257-86del ENSP00000502375.1:n.257-86del
ENST00000255078.7:c.257-86del ENSP00000255078.3:n.257-86del
ENST00000539224.1:c.257-86del ENSP00000440465.1:n.257-86del
ENST00000544541.1:c.87-86del ENSP00000443343.1:n.87-86del
ENST00000545146.1:c.*127-86del ENSP00000456366.1:n.*127-86del
NM_002180.2:c.257-86del , LRG_250t1:c.257-86del NP_002171.2:n.257-86del
XM_005273974.2:c.-755-86del XP_005274031.1:n.-755-86del
XM_005273976.1:c.257-86del XP_005274033.1:n.257-86del
XR_247198.1:n.359-86del
XR_949903.1:n.359-86del
XM_005273976.2:c.257-86del XP_005274033.1:n.257-86del
XM_017017669.2:c.-657-86del XP_016873158.1:n.-657-86del
XM_017017671.2:c.257-86del XP_016873160.1:n.257-86del
XR_949903.3:n.355-86del
NM_002180.3:c.257-86del MANE Select NP_002171.2:n.257-86del