Canonical Allele Identifier: CA2614746236
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68908164del , CM000673.2:g.68908164del GRCh38
NC_000011.9:g.68675632del , CM000673.1:g.68675632del GRCh37
NC_000011.8:g.68432208del NCBI36
NG_007976.1:g.9314del , LRG_250:g.9314del

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.276del MANE Select ENSP00000255078.4:p.Tyr92Ter
ENST00000539224.2:c.239del
ENST00000674583.1:c.239del
ENST00000674597.1:c.87del
ENST00000674955.1:c.276del ENSP00000502463.1:p.Tyr92Ter
ENST00000675142.1:n.239del
ENST00000675469.1:c.152del
ENST00000675615.1:c.276del ENSP00000502413.1:p.Tyr92Ter
ENST00000675674.1:n.239del
ENST00000675873.1:c.239del
ENST00000676173.1:n.320del
ENST00000676228.1:c.276del ENSP00000502375.1:p.Tyr92Ter
ENST00000255078.7:c.276del ENSP00000255078.3:p.Tyr92Ter
ENST00000539224.1:c.276del ENSP00000440465.1:p.Tyr92Ter
ENST00000544541.1:c.*16del ENSP00000443343.1:n.*16del
ENST00000545146.1:c.*146del ENSP00000456366.1:n.*146del
NM_002180.2:c.276del , LRG_250t1:c.276del NP_002171.2:p.Tyr92Ter
XM_005273974.2:c.-736del XP_005274031.1:n.-736del
XM_005273976.1:c.276del XP_005274033.1:p.Tyr92Ter
XR_247198.1:n.378del
XR_949903.1:n.378del
XM_005273976.2:c.276del XP_005274033.1:p.Tyr92Ter
XM_017017669.2:c.-638del XP_016873158.1:n.-638del
XM_017017671.2:c.276del XP_016873160.1:p.Tyr92Ter
XR_949903.3:n.374del
NM_002180.3:c.276del MANE Select NP_002171.2:p.Tyr92Ter