Canonical Allele Identifier: CA2690632285

Gene: ROR2

Linked Data

• gnomAD v4: 9-91723927-ACCATCTGAGGAGGCACCTGCTGCGGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723935_91723961del , CM000671.2:g.91723935_91723961del	GRCh38
NC_000009.11:g.94486217_94486243del , CM000671.1:g.94486217_94486243del	GRCh37
NC_000009.10:g.93526038_93526064del	NCBI36
NG_008089.1:g.231209_231235del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2540_2566del MANE Select	ENSP00000364860.3:p.Ala847_Met855del
ENST00000375708.3:c.2540_2566del	ENSP00000364860.3:p.Ala847_Met855del
ENST00000375715.5:c.1920+200_1920+226del	ENSP00000364867.1:n.1920+200_1920+226del
ENST00000550066.5:n.3008_3034del
NM_004560.3:c.2540_2566del	NP_004551.2:p.Ala847_Met855del
XM_005252008.3:c.2120_2146del	XP_005252065.1:p.Ala707_Met715del
XM_005252009.3:c.1337_1363del	XP_005252066.1:p.Ala446_Met454del
XM_006717121.2:c.2120_2146del	XP_006717184.1:p.Ala707_Met715del
XM_011518721.1:c.2120_2146del	XP_011517023.1:p.Ala707_Met715del
XM_005252008.4:c.2120_2146del	XP_005252065.1:p.Ala707_Met715del
XM_006717121.3:c.2120_2146del	XP_006717184.1:p.Ala707_Met715del
XM_017014762.1:c.2531_2557del	XP_016870251.1:p.Ala844_Met852del
XM_017014763.1:c.2120_2146del	XP_016870252.1:p.Ala707_Met715del
NM_004560.4:c.2540_2566del MANE Select	NP_004551.2:p.Ala847_Met855del