Canonical Allele Identifier: CA15746993

Gene: BIN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51310050A>G , CM000674.2:g.51310050A>G	GRCh38
NC_000012.11:g.51703834A>G , CM000674.1:g.51703834A>G	GRCh37
NC_000012.10:g.49990101A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452142.7:c.162+3773T>C	ENSP00000410217.3:n.162+3773T>C
ENST00000604560.6:c.82-6909T>C	ENSP00000474972.3:n.82-6909T>C
ENST00000615107.6:c.162+3773T>C MANE Select	ENSP00000483983.2:n.162+3773T>C
ENST00000452142.6:c.214+3773T>C
ENST00000544402.5:c.84+3773T>C	ENSP00000445874.1:n.84+3773T>C
ENST00000604560.5:c.95-6909T>C
ENST00000605039.5:n.214+3773T>C
ENST00000605423.1:c.202+3773T>C
ENST00000615107.4:c.258+3773T>C	ENSP00000483983.1:n.258+3773T>C
NM_001290007.1:c.84+3773T>C	NP_001276936.1:n.84+3773T>C
NM_001290008.1:c.258+3773T>C	NP_001276937.1:n.258+3773T>C
NM_001290009.1:c.-781+3773T>C	NP_001276938.1:n.-781+3773T>C
NM_016293.3:c.258+3773T>C	NP_057377.3:n.258+3773T>C
XM_005268957.2:c.258+3773T>C	XP_005269014.1:n.258+3773T>C
XM_005268958.2:c.258+3773T>C	XP_005269015.1:n.258+3773T>C
XM_011538452.1:c.258+3773T>C	XP_011536754.1:n.258+3773T>C
NM_001290007.2:c.84+3773T>C	NP_001276936.1:n.84+3773T>C
NM_001290008.2:c.162+3773T>C	NP_001276937.2:n.162+3773T>C
NM_001290009.2:c.-781+3773T>C	NP_001276938.1:n.-781+3773T>C
NM_001364779.1:c.162+3773T>C	NP_001351708.1:n.162+3773T>C
NM_001364780.1:c.162+3773T>C	NP_001351709.1:n.162+3773T>C
NM_001364781.1:c.162+3773T>C	NP_001351710.1:n.162+3773T>C
NM_016293.4:c.162+3773T>C MANE Select	NP_057377.4:n.162+3773T>C
XM_024449016.1:c.-379+3773T>C	XP_024304784.1:n.-379+3773T>C
XR_001748746.1:n.258+3773T>C