Canonical Allele Identifier: CA2614746112
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68915138_68915139insCTG , CM000673.2:g.68915138_68915139insCTG GRCh38
NC_000011.9:g.68682606_68682607insCTG , CM000673.1:g.68682606_68682607insCTG GRCh37
NC_000011.8:g.68439182_68439183insCTG NCBI36
NG_007976.1:g.16288_16289insCTG , LRG_250:g.16288_16289insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.912+115_912+116insCTG MANE Select ENSP00000255078.4:n.912+115_912+116insCTG
ENST00000539224.2:c.1041+115_1041+116insCTG
ENST00000674955.1:c.912+115_912+116insCTG ENSP00000502463.1:n.912+115_912+116insCTG
ENST00000675118.1:c.259+115_259+116insCTG
ENST00000675119.1:c.201+115_201+116insCTG ENSP00000501861.1:n.201+115_201+116insCTG
ENST00000675305.1:c.201+115_201+116insCTG ENSP00000502365.1:n.201+115_201+116insCTG
ENST00000675464.1:c.195+121_195+122insCTG ENSP00000502650.1:n.195+121_195+122insCTG
ENST00000675615.1:c.912+115_912+116insCTG ENSP00000502413.1:n.912+115_912+116insCTG
ENST00000675683.1:c.299+115_299+116insCTG
ENST00000676173.1:n.956+115_956+116insCTG
ENST00000676228.1:c.*235+115_*235+116insCTG ENSP00000502375.1:n.*235+115_*235+116insCTG
ENST00000255078.7:c.912+115_912+116insCTG ENSP00000255078.3:n.912+115_912+116insCTG
NM_002180.2:c.912+115_912+116insCTG , LRG_250t1:c.912+115_912+116insCTG NP_002171.2:n.912+115_912+116insCTG
XM_005273974.2:c.-100+115_-100+116insCTG XP_005274031.1:n.-100+115_-100+116insCTG
XM_005273976.1:c.912+115_912+116insCTG XP_005274033.1:n.912+115_912+116insCTG
XR_247198.1:n.1014+115_1014+116insCTG
XR_949903.1:n.1014+115_1014+116insCTG
XM_005273976.2:c.912+115_912+116insCTG XP_005274033.1:n.912+115_912+116insCTG
XM_017017669.2:c.-100+115_-100+116insCTG XP_016873158.1:n.-100+115_-100+116insCTG
XM_017017670.2:c.-100+115_-100+116insCTG XP_016873159.1:n.-100+115_-100+116insCTG
XM_017017671.2:c.912+115_912+116insCTG XP_016873160.1:n.912+115_912+116insCTG
XR_949903.3:n.1010+115_1010+116insCTG
NM_002180.3:c.912+115_912+116insCTG MANE Select NP_002171.2:n.912+115_912+116insCTG