Canonical Allele Identifier: CA1863922904
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91724530G= , CM000671.2:g.91724530G= GRCh38
NC_000009.11:g.94486812G= , CM000671.1:g.94486812G= GRCh37
NC_000009.10:g.93526633G= NCBI36
NG_008089.1:g.230633C=

Transcript Alleles

HGVS Amino-acid change
ENST00000375708.4:c.1964C= MANE Select ENSP00000364860.3:p.Pro655=
ENST00000375708.3:c.1964C= ENSP00000364860.3:p.Pro655=
ENST00000375715.5:c.1544C= ENSP00000364867.1:p.Pro515=
ENST00000550066.5:n.2432C=
NM_004560.3:c.1964C= NP_004551.2:p.Pro655=
XM_005252008.3:c.1544C= XP_005252065.1:p.Pro515=
XM_005252009.3:c.761C= XP_005252066.1:p.Pro254=
XM_006717121.2:c.1544C= XP_006717184.1:p.Pro515=
XM_011518721.1:c.1544C= XP_011517023.1:p.Pro515=
XM_005252008.4:c.1544C= XP_005252065.1:p.Pro515=
XM_006717121.3:c.1544C= XP_006717184.1:p.Pro515=
XM_017014762.1:c.1955C= XP_016870251.1:p.Pro652=
XM_017014763.1:c.1544C= XP_016870252.1:p.Pro515=
NM_004560.4:c.1964C= MANE Select NP_004551.2:p.Pro655=