Canonical Allele Identifier: CA5120409
Community Standard Title: NM_004560.4(ROR2):c.2382G>A (p.Pro794=)
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91724112C>T , CM000671.2:g.91724112C>T GRCh38
NC_000009.11:g.94486394C>T , CM000671.1:g.94486394C>T GRCh37
NC_000009.10:g.93526215C>T NCBI36
NG_008089.1:g.231051G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004560.4:c.2382G>A MANE Select NP_004551.2:p.Pro794=
ENST00000375708.4:c.2382G>A MANE Select ENSP00000364860.3:p.Pro794=
NM_004560.3:c.2382G>A NP_004551.2:p.Pro794=
ENST00000375708.3:c.2382G>A ENSP00000364860.3:p.Pro794=
ENST00000375715.5:c.1920+42G>A ENSP00000364867.1:n.1920+42G>A
ENST00000550066.5:n.2850G>A
XM_005252008.3:c.1962G>A XP_005252065.1:p.Pro654=
XM_005252008.4:c.1962G>A XP_005252065.1:p.Pro654=
XM_005252009.3:c.1179G>A XP_005252066.1:p.Pro393=
XM_006717121.2:c.1962G>A XP_006717184.1:p.Pro654=
XM_006717121.3:c.1962G>A XP_006717184.1:p.Pro654=
XM_011518721.1:c.1962G>A XP_011517023.1:p.Pro654=
XM_017014762.1:c.2373G>A XP_016870251.1:p.Pro791=
XM_017014763.1:c.1962G>A XP_016870252.1:p.Pro654=