Canonical Allele Identifier: CA2167016550
Community Standard Title: NM_015307.2(ENTREP2):c.277-55321G=
Gene: ENTREP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.29307799C= , CM000677.2:g.29307799C= GRCh38
NC_000015.9:g.29600003C= , CM000677.1:g.29600003C= GRCh37
NC_000015.8:g.27387295C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015307.2:c.277-55321G= MANE Select NP_056122.1:n.277-55321G=
ENST00000261275.5:c.277-55321G= MANE Select ENSP00000261275.4:n.277-55321G=
NM_001387214.1:c.277-55321G= NP_001374143.1:n.277-55321G=
NM_001387215.1:c.-12-55321G= NP_001374144.1:n.-12-55321G=
NM_001387216.1:c.-12-55321G= NP_001374145.1:n.-12-55321G=
NM_001387217.1:c.-12-55321G= NP_001374146.1:n.-12-55321G=
NM_015307.1:c.277-55321G= NP_056122.1:n.277-55321G=
ENST00000261275.4:c.277-55321G= ENSP00000261275.4:n.277-55321G=
ENST00000560082.1:c.-12-55321G= ENSP00000452860.1:n.-12-55321G=
XM_011521407.1:c.160-55321G= XP_011519709.1:n.160-55321G=
XM_011521407.2:c.160-55321G= XP_011519709.1:n.160-55321G=