Canonical Allele Identifier: CA2574904374

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933745_68933746del , CM000673.2:g.68933745_68933746del	GRCh38
NC_000011.9:g.68701213_68701214del , CM000673.1:g.68701213_68701214del	GRCh37
NC_000011.8:g.68457789_68457790del	NCBI36
NG_007976.1:g.34895_34896del , LRG_250:g.34895_34896del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1419-50_1419-49del MANE Select	ENSP00000255078.4:n.1419-50_1419-49del
ENST00000674955.1:c.*136-50_*136-49del	ENSP00000502463.1:n.*136-50_*136-49del
ENST00000675118.1:c.907-50_907-49del
ENST00000675205.1:n.183+264_183+265del
ENST00000675615.1:c.1419-50_1419-49del	ENSP00000502413.1:n.1419-50_1419-49del
ENST00000675648.1:n.794-50_794-49del
ENST00000675997.1:n.113-719_113-718del
ENST00000676173.1:n.2164-50_2164-49del
ENST00000676228.1:c.*742-50_*742-49del	ENSP00000502375.1:n.*742-50_*742-49del
ENST00000255078.7:c.1419-50_1419-49del	ENSP00000255078.3:n.1419-50_1419-49del
ENST00000537458.5:n.536-50_536-49del
ENST00000539064.5:n.1178-50_1178-49del
ENST00000541229.5:n.64_65del
ENST00000543739.5:n.536-50_536-49del
NM_002180.2:c.1419-50_1419-49del , LRG_250t1:c.1419-50_1419-49del	NP_002171.2:n.1419-50_1419-49del
XM_005273974.2:c.408-50_408-49del	XP_005274031.1:n.408-50_408-49del
XM_005273975.2:c.291-50_291-49del	XP_005274032.1:n.291-50_291-49del
XM_011544994.1:c.186-50_186-49del	XP_011543296.1:n.186-50_186-49del
XR_949903.1:n.1521-50_1521-49del
XM_005273975.3:c.291-50_291-49del	XP_005274032.1:n.291-50_291-49del
XM_017017669.2:c.408-50_408-49del	XP_016873158.1:n.408-50_408-49del
XM_017017670.2:c.408-50_408-49del	XP_016873159.1:n.408-50_408-49del
XM_017017671.2:c.1419-50_1419-49del	XP_016873160.1:n.1419-50_1419-49del
XR_949903.3:n.1517-50_1517-49del
NM_002180.3:c.1419-50_1419-49del MANE Select	NP_002171.2:n.1419-50_1419-49del