Canonical Allele Identifier: CA2167016549
Gene: ENTREP2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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