Canonical Allele Identifier: CA2803546364
Gene: ENTREP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.29132470C>A , CM000677.2:g.29132470C>A GRCh38
NC_000015.9:g.29424673C>A , CM000677.1:g.29424673C>A GRCh37
NC_000015.8:g.27211965C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261275.5:c.928-3606G>T MANE Select ENSP00000261275.4:n.928-3606G>T
ENST00000261275.4:c.928-3606G>T ENSP00000261275.4:n.928-3606G>T
ENST00000560021.1:n.664-3606G>T
NM_015307.1:c.928-3606G>T NP_056122.1:n.928-3606G>T
XM_011521407.1:c.1039-3606G>T XP_011519709.1:n.1039-3606G>T
XM_011521407.2:c.1039-3606G>T XP_011519709.1:n.1039-3606G>T
NM_001387214.1:c.793-3606G>T NP_001374143.1:n.793-3606G>T
NM_001387215.1:c.640-3606G>T NP_001374144.1:n.640-3606G>T
NM_001387216.1:c.640-3606G>T NP_001374145.1:n.640-3606G>T
NM_001387217.1:c.505-3606G>T NP_001374146.1:n.505-3606G>T
NM_015307.2:c.928-3606G>T MANE Select NP_056122.1:n.928-3606G>T