Canonical Allele Identifier: CA2166933147

Gene: ENTREP2

Linked Data

• dbSNP Id: rs2045694381

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.29132602_29132603del , CM000677.2:g.29132602_29132603del	GRCh38
NC_000015.9:g.29424805_29424806del , CM000677.1:g.29424805_29424806del	GRCh37
NC_000015.8:g.27212097_27212098del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261275.5:c.928-3735_928-3734del MANE Select	ENSP00000261275.4:n.928-3735_928-3734del
ENST00000261275.4:c.928-3735_928-3734del	ENSP00000261275.4:n.928-3735_928-3734del
ENST00000560021.1:n.664-3735_664-3734del
NM_015307.1:c.928-3735_928-3734del	NP_056122.1:n.928-3735_928-3734del
XM_011521407.1:c.1039-3735_1039-3734del	XP_011519709.1:n.1039-3735_1039-3734del
XM_011521407.2:c.1039-3735_1039-3734del	XP_011519709.1:n.1039-3735_1039-3734del
NM_001387214.1:c.793-3735_793-3734del	NP_001374143.1:n.793-3735_793-3734del
NM_001387215.1:c.640-3735_640-3734del	NP_001374144.1:n.640-3735_640-3734del
NM_001387216.1:c.640-3735_640-3734del	NP_001374145.1:n.640-3735_640-3734del
NM_001387217.1:c.505-3735_505-3734del	NP_001374146.1:n.505-3735_505-3734del
NM_015307.2:c.928-3735_928-3734del MANE Select	NP_056122.1:n.928-3735_928-3734del