Canonical Allele Identifier: CA616739485
Gene: ENTREP2 HGNC NCBI

Linked Data

dbSNP Id: rs1300550686

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.29132584_29132587del , CM000677.2:g.29132584_29132587del GRCh38
NC_000015.9:g.29424787_29424790del , CM000677.1:g.29424787_29424790del GRCh37
NC_000015.8:g.27212079_27212082del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261275.5:c.928-3720_928-3717del MANE Select ENSP00000261275.4:n.928-3720_928-3717del
ENST00000261275.4:c.928-3720_928-3717del ENSP00000261275.4:n.928-3720_928-3717del
ENST00000560021.1:n.664-3720_664-3717del
NM_015307.1:c.928-3720_928-3717del NP_056122.1:n.928-3720_928-3717del
XM_011521407.1:c.1039-3720_1039-3717del XP_011519709.1:n.1039-3720_1039-3717del
XM_011521407.2:c.1039-3720_1039-3717del XP_011519709.1:n.1039-3720_1039-3717del
NM_001387214.1:c.793-3720_793-3717del NP_001374143.1:n.793-3720_793-3717del
NM_001387215.1:c.640-3720_640-3717del NP_001374144.1:n.640-3720_640-3717del
NM_001387216.1:c.640-3720_640-3717del NP_001374145.1:n.640-3720_640-3717del
NM_001387217.1:c.505-3720_505-3717del NP_001374146.1:n.505-3720_505-3717del
NM_015307.2:c.928-3720_928-3717del MANE Select NP_056122.1:n.928-3720_928-3717del