Canonical Allele Identifier: CA2838483501

Gene: BIN3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22635900del , CM000670.2:g.22635900del	GRCh38
NC_000008.10:g.22493413del , CM000670.1:g.22493413del	GRCh37
NC_000008.9:g.22549358del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276416.11:c.160+627del MANE Select	ENSP00000276416.6:n.160+627del
ENST00000640731.1:c.160+627del	ENSP00000492772.1:n.160+627del
ENST00000276416.10:c.160+627del	ENSP00000276416.6:n.160+627del
ENST00000399977.8:c.16+1024del	ENSP00000382859.4:n.16+1024del
ENST00000519335.5:n.139+627del
ENST00000519513.5:c.-2-5320del	ENSP00000430423.1:n.-2-5320del
ENST00000519863.5:n.153+627del
ENST00000520292.1:c.160+627del	ENSP00000429660.1:n.160+627del
ENST00000521140.1:n.153+627del
ENST00000522687.5:c.160+627del	ENSP00000430546.1:n.160+627del
NM_018688.4:c.160+627del	NP_061158.1:n.160+627del
XM_005273573.2:c.16+1024del	XP_005273630.1:n.16+1024del
XM_011544586.1:c.-116+627del	XP_011542888.1:n.-116+627del
XM_011544587.1:c.160+627del	XP_011542889.1:n.160+627del
XR_949444.1:n.257+627del
NM_001363046.1:c.16+1024del	NP_001349975.1:n.16+1024del
NM_018688.5:c.160+627del	NP_061158.1:n.160+627del
NR_156436.1:n.257+627del
XM_011544586.2:c.-116+627del	XP_011542888.1:n.-116+627del
NM_018688.6:c.160+627del MANE Select	NP_061158.1:n.160+627del
NM_001363046.2:c.16+1024del	NP_001349975.1:n.16+1024del
NR_156436.2:n.230+627del