Canonical Allele Identifier: CA2573144754

Gene: ROR2

Linked Data

• ClinVar Variation Id: 1390956
• ClinVar RCV Id: RCV001891249
• dbSNP Id: rs2118608399
• gnomAD v4: 9-91723976-CCGGGTAGAAGTTGGGCAGGTAGGCCCCATAGGCCGGCACCGGCTGGTAGCCGTTGACGGGGACGTAGAGCTGCGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723981_91724055del , CM000671.2:g.91723981_91724055del	GRCh38
NC_000009.11:g.94486263_94486337del , CM000671.1:g.94486263_94486337del	GRCh37
NC_000009.10:g.93526084_93526158del	NCBI36
NG_008089.1:g.231112_231186del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2443_2517del MANE Select	ENSP00000364860.3:p.Pro815_Pro839del
ENST00000375708.3:c.2443_2517del	ENSP00000364860.3:p.Pro815_Pro839del
ENST00000375715.5:c.1920+103_1920+177del	ENSP00000364867.1:n.1920+103_1920+177del
ENST00000550066.5:n.2911_2985del
NM_004560.3:c.2443_2517del	NP_004551.2:p.Pro815_Pro839del
XM_005252008.3:c.2023_2097del	XP_005252065.1:p.Pro675_Pro699del
XM_005252009.3:c.1240_1314del	XP_005252066.1:p.Pro414_Pro438del
XM_006717121.2:c.2023_2097del	XP_006717184.1:p.Pro675_Pro699del
XM_011518721.1:c.2023_2097del	XP_011517023.1:p.Pro675_Pro699del
XM_005252008.4:c.2023_2097del	XP_005252065.1:p.Pro675_Pro699del
XM_006717121.3:c.2023_2097del	XP_006717184.1:p.Pro675_Pro699del
XM_017014762.1:c.2434_2508del	XP_016870251.1:p.Pro812_Pro836del
XM_017014763.1:c.2023_2097del	XP_016870252.1:p.Pro675_Pro699del
NM_004560.4:c.2443_2517del MANE Select	NP_004551.2:p.Pro815_Pro839del