Canonical Allele Identifier: CA2614750099
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68934065_68934066del , CM000673.2:g.68934065_68934066del GRCh38
NC_000011.9:g.68701533_68701534del , CM000673.1:g.68701533_68701534del GRCh37
NC_000011.8:g.68458109_68458110del NCBI36
NG_007976.1:g.35215_35216del , LRG_250:g.35215_35216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.1537+152_1537+153del MANE Select ENSP00000255078.4:n.1537+152_1537+153del
ENST00000674955.1:c.*254+152_*254+153del ENSP00000502463.1:n.*254+152_*254+153del
ENST00000675118.1:c.1025+152_1025+153del
ENST00000675205.1:n.184-399_184-398del
ENST00000675615.1:c.1537+152_1537+153del ENSP00000502413.1:n.1537+152_1537+153del
ENST00000675648.1:n.912+152_912+153del
ENST00000675997.1:n.113-399_113-398del
ENST00000676173.1:n.2282+152_2282+153del
ENST00000676228.1:c.*860+152_*860+153del ENSP00000502375.1:n.*860+152_*860+153del
ENST00000255078.7:c.1537+152_1537+153del ENSP00000255078.3:n.1537+152_1537+153del
ENST00000537458.5:n.806_807del
ENST00000539064.5:n.1296+152_1296+153del
ENST00000541229.5:n.232+152_232+153del
ENST00000543739.5:n.654+152_654+153del
NM_002180.2:c.1537+152_1537+153del , LRG_250t1:c.1537+152_1537+153del NP_002171.2:n.1537+152_1537+153del
XM_005273974.2:c.526+152_526+153del XP_005274031.1:n.526+152_526+153del
XM_005273975.2:c.409+152_409+153del XP_005274032.1:n.409+152_409+153del
XM_011544994.1:c.304+152_304+153del XP_011543296.1:n.304+152_304+153del
XR_949903.1:n.1639+152_1639+153del
XM_005273975.3:c.409+152_409+153del XP_005274032.1:n.409+152_409+153del
XM_017017669.2:c.526+152_526+153del XP_016873158.1:n.526+152_526+153del
XM_017017670.2:c.526+152_526+153del XP_016873159.1:n.526+152_526+153del
XM_017017671.2:c.1537+152_1537+153del XP_016873160.1:n.1537+152_1537+153del
XR_949903.3:n.1635+152_1635+153del
NM_002180.3:c.1537+152_1537+153del MANE Select NP_002171.2:n.1537+152_1537+153del