Canonical Allele Identifier: CA1653702549
Gene: BEND3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107079222_107079227delinsCCCGGG , CM000668.2:g.107079222_107079227delinsCCCGGG GRCh38
NC_000006.11:g.107400426_107400431delinsCCCGGG , CM000668.1:g.107400426_107400431delinsCCCGGG GRCh37
NC_000006.10:g.107507119_107507124delinsCCCGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369042.6:c.241-8277_241-8272delinsCCCGGG MANE Select ENSP00000358038.1:n.241-8277_241-8272delinsCCCGGG
ENST00000369042.5:c.241-8277_241-8272delinsCCCGGG ENSP00000358038.1:n.241-8277_241-8272delinsCCCGGG
ENST00000429433.3:c.241-8277_241-8272delinsCCCGGG ENSP00000411268.2:n.241-8277_241-8272delinsCCCGGG
NM_001080450.2:c.241-8277_241-8272delinsCCCGGG NP_001073919.1:n.241-8277_241-8272delinsCCCGGG
XM_005267079.2:c.241-8277_241-8272delinsCCCGGG XP_005267136.1:n.241-8277_241-8272delinsCCCGGG
XM_005267080.2:c.241-8277_241-8272delinsCCCGGG XP_005267137.1:n.241-8277_241-8272delinsCCCGGG
XM_011536005.1:c.241-8277_241-8272delinsCCCGGG XP_011534307.1:n.241-8277_241-8272delinsCCCGGG
XM_011536006.1:c.241-8277_241-8272delinsCCCGGG XP_011534308.1:n.241-8277_241-8272delinsCCCGGG
XM_011536007.1:c.241-8277_241-8272delinsCCCGGG XP_011534309.1:n.241-8277_241-8272delinsCCCGGG
XM_005267079.4:c.241-8277_241-8272delinsCCCGGG XP_005267136.1:n.241-8277_241-8272delinsCCCGGG
XM_005267080.4:c.241-8277_241-8272delinsCCCGGG XP_005267137.1:n.241-8277_241-8272delinsCCCGGG
XM_011536005.3:c.241-8277_241-8272delinsCCCGGG XP_011534307.1:n.241-8277_241-8272delinsCCCGGG
NM_001367314.1:c.241-8277_241-8272delinsCCCGGG MANE Select NP_001354243.1:n.241-8277_241-8272delinsCCCGGG
NM_001080450.3:c.241-8277_241-8272delinsCCCGGG NP_001073919.1:n.241-8277_241-8272delinsCCCGGG