Canonical Allele Identifier: CA373799244

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488824T>G (hg19) ; chr9:g.91726542T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726542T>G , CM000671.2:g.91726542T>G	GRCh38
NC_000009.11:g.94488824T>G , CM000671.1:g.94488824T>G	GRCh37
NC_000009.10:g.93528645T>G	NCBI36
NG_008089.1:g.228621A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1385A>C MANE Select	ENSP00000364860.3:p.Gln462Pro
ENST00000375708.3:c.1385A>C	ENSP00000364860.3:p.Gln462Pro
ENST00000375715.5:c.965A>C	ENSP00000364867.1:p.Gln322Pro
ENST00000550066.5:n.1853A>C
NM_004560.3:c.1385A>C	NP_004551.2:p.Gln462Pro
XM_005252008.3:c.965A>C	XP_005252065.1:p.Gln322Pro
XM_005252009.3:c.182A>C	XP_005252066.1:p.Gln61Pro
XM_006717121.2:c.965A>C	XP_006717184.1:p.Gln322Pro
XM_011518721.1:c.965A>C	XP_011517023.1:p.Gln322Pro
NM_001318204.1:c.*52A>C	NP_001305133.1:n.*52A>C
XM_005252008.4:c.965A>C	XP_005252065.1:p.Gln322Pro
XM_006717121.3:c.965A>C	XP_006717184.1:p.Gln322Pro
XM_017014762.1:c.1376A>C	XP_016870251.1:p.Gln459Pro
XM_017014763.1:c.965A>C	XP_016870252.1:p.Gln322Pro
XR_001746315.1:n.1594A>C
NM_004560.4:c.1385A>C MANE Select	NP_004551.2:p.Gln462Pro
NM_001318204.2:c.*52A>C	NP_001305133.1:n.*52A>C