Canonical Allele Identifier: CA373794268

Gene: ROR2

Linked Data

• gnomAD v4: 9-91724045-G-T
• MyVariant Identifiers: chr9:g.94486327G>T (hg19) ; chr9:g.91724045G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724045G>T , CM000671.2:g.91724045G>T	GRCh38
NC_000009.11:g.94486327G>T , CM000671.1:g.94486327G>T	GRCh37
NC_000009.10:g.93526148G>T	NCBI36
NG_008089.1:g.231118C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2449C>A MANE Select	ENSP00000364860.3:p.Leu817Ile
ENST00000375708.3:c.2449C>A	ENSP00000364860.3:p.Leu817Ile
ENST00000375715.5:c.1920+109C>A	ENSP00000364867.1:n.1920+109C>A
ENST00000550066.5:n.2917C>A
NM_004560.3:c.2449C>A	NP_004551.2:p.Leu817Ile
XM_005252008.3:c.2029C>A	XP_005252065.1:p.Leu677Ile
XM_005252009.3:c.1246C>A	XP_005252066.1:p.Leu416Ile
XM_006717121.2:c.2029C>A	XP_006717184.1:p.Leu677Ile
XM_011518721.1:c.2029C>A	XP_011517023.1:p.Leu677Ile
XM_005252008.4:c.2029C>A	XP_005252065.1:p.Leu677Ile
XM_006717121.3:c.2029C>A	XP_006717184.1:p.Leu677Ile
XM_017014762.1:c.2440C>A	XP_016870251.1:p.Leu814Ile
XM_017014763.1:c.2029C>A	XP_016870252.1:p.Leu677Ile
NM_004560.4:c.2449C>A MANE Select	NP_004551.2:p.Leu817Ile