Canonical Allele Identifier: CA2530438875
Gene: BEND3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107079236_107079237insTAT , CM000668.2:g.107079236_107079237insTAT GRCh38
NC_000006.11:g.107400440_107400441insTAT , CM000668.1:g.107400440_107400441insTAT GRCh37
NC_000006.10:g.107507133_107507134insTAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369042.6:c.241-8287_241-8286insATA MANE Select ENSP00000358038.1:n.241-8287_241-8286insATA
ENST00000369042.5:c.241-8287_241-8286insATA ENSP00000358038.1:n.241-8287_241-8286insATA
ENST00000429433.3:c.241-8287_241-8286insATA ENSP00000411268.2:n.241-8287_241-8286insATA
NM_001080450.2:c.241-8287_241-8286insATA NP_001073919.1:n.241-8287_241-8286insATA
XM_005267079.2:c.241-8287_241-8286insATA XP_005267136.1:n.241-8287_241-8286insATA
XM_005267080.2:c.241-8287_241-8286insATA XP_005267137.1:n.241-8287_241-8286insATA
XM_011536005.1:c.241-8287_241-8286insATA XP_011534307.1:n.241-8287_241-8286insATA
XM_011536006.1:c.241-8287_241-8286insATA XP_011534308.1:n.241-8287_241-8286insATA
XM_011536007.1:c.241-8287_241-8286insATA XP_011534309.1:n.241-8287_241-8286insATA
XM_005267079.4:c.241-8287_241-8286insATA XP_005267136.1:n.241-8287_241-8286insATA
XM_005267080.4:c.241-8287_241-8286insATA XP_005267137.1:n.241-8287_241-8286insATA
XM_011536005.3:c.241-8287_241-8286insATA XP_011534307.1:n.241-8287_241-8286insATA
NM_001367314.1:c.241-8287_241-8286insATA MANE Select NP_001354243.1:n.241-8287_241-8286insATA
NM_001080450.3:c.241-8287_241-8286insATA NP_001073919.1:n.241-8287_241-8286insATA