Canonical Allele Identifier: CA373793109
Gene: ROR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91723722C>G , CM000671.2:g.91723722C>G GRCh38
NC_000009.11:g.94486004C>G , CM000671.1:g.94486004C>G GRCh37
NC_000009.10:g.93525825C>G NCBI36
NG_008089.1:g.231441G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.2772G>C MANE Select ENSP00000364860.3:p.Glu924Asp
ENST00000375708.3:c.2772G>C ENSP00000364860.3:p.Glu924Asp
ENST00000375715.5:c.1920+432G>C ENSP00000364867.1:n.1920+432G>C
ENST00000550066.5:n.3240G>C
NM_004560.3:c.2772G>C NP_004551.2:p.Glu924Asp
XM_005252008.3:c.2352G>C XP_005252065.1:p.Glu784Asp
XM_005252009.3:c.1569G>C XP_005252066.1:p.Glu523Asp
XM_006717121.2:c.2352G>C XP_006717184.1:p.Glu784Asp
XM_011518721.1:c.2352G>C XP_011517023.1:p.Glu784Asp
XM_005252008.4:c.2352G>C XP_005252065.1:p.Glu784Asp
XM_006717121.3:c.2352G>C XP_006717184.1:p.Glu784Asp
XM_017014762.1:c.2763G>C XP_016870251.1:p.Glu921Asp
XM_017014763.1:c.2352G>C XP_016870252.1:p.Glu784Asp
NM_004560.4:c.2772G>C MANE Select NP_004551.2:p.Glu924Asp