Canonical Allele Identifier: CA373793341

Gene: ROR2

Linked Data

• gnomAD v4: 9-91723829-G-T
• MyVariant Identifiers: chr9:g.94486111G>T (hg19) ; chr9:g.91723829G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723829G>T , CM000671.2:g.91723829G>T	GRCh38
NC_000009.11:g.94486111G>T , CM000671.1:g.94486111G>T	GRCh37
NC_000009.10:g.93525932G>T	NCBI36
NG_008089.1:g.231334C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2665C>A MANE Select	ENSP00000364860.3:p.Leu889Met
ENST00000375708.3:c.2665C>A	ENSP00000364860.3:p.Leu889Met
ENST00000375715.5:c.1920+325C>A	ENSP00000364867.1:n.1920+325C>A
ENST00000550066.5:n.3133C>A
NM_004560.3:c.2665C>A	NP_004551.2:p.Leu889Met
XM_005252008.3:c.2245C>A	XP_005252065.1:p.Leu749Met
XM_005252009.3:c.1462C>A	XP_005252066.1:p.Leu488Met
XM_006717121.2:c.2245C>A	XP_006717184.1:p.Leu749Met
XM_011518721.1:c.2245C>A	XP_011517023.1:p.Leu749Met
XM_005252008.4:c.2245C>A	XP_005252065.1:p.Leu749Met
XM_006717121.3:c.2245C>A	XP_006717184.1:p.Leu749Met
XM_017014762.1:c.2656C>A	XP_016870251.1:p.Leu886Met
XM_017014763.1:c.2245C>A	XP_016870252.1:p.Leu749Met
NM_004560.4:c.2665C>A MANE Select	NP_004551.2:p.Leu889Met