Canonical Allele Identifier: CA2166933146
Gene: ENTREP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.29132597_29132599delinsTGA , CM000677.2:g.29132597_29132599delinsTGA GRCh38
NC_000015.9:g.29424800_29424802delinsTGA , CM000677.1:g.29424800_29424802delinsTGA GRCh37
NC_000015.8:g.27212092_27212094delinsTGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261275.5:c.928-3735_928-3733delinsTCA MANE Select ENSP00000261275.4:n.928-3735_928-3733delinsTCA
ENST00000261275.4:c.928-3735_928-3733delinsTCA ENSP00000261275.4:n.928-3735_928-3733delinsTCA
ENST00000560021.1:n.664-3735_664-3733delinsTCA
NM_015307.1:c.928-3735_928-3733delinsTCA NP_056122.1:n.928-3735_928-3733delinsTCA
XM_011521407.1:c.1039-3735_1039-3733delinsTCA XP_011519709.1:n.1039-3735_1039-3733delinsTCA
XM_011521407.2:c.1039-3735_1039-3733delinsTCA XP_011519709.1:n.1039-3735_1039-3733delinsTCA
NM_001387214.1:c.793-3735_793-3733delinsTCA NP_001374143.1:n.793-3735_793-3733delinsTCA
NM_001387215.1:c.640-3735_640-3733delinsTCA NP_001374144.1:n.640-3735_640-3733delinsTCA
NM_001387216.1:c.640-3735_640-3733delinsTCA NP_001374145.1:n.640-3735_640-3733delinsTCA
NM_001387217.1:c.505-3735_505-3733delinsTCA NP_001374146.1:n.505-3735_505-3733delinsTCA
NM_015307.2:c.928-3735_928-3733delinsTCA MANE Select NP_056122.1:n.928-3735_928-3733delinsTCA