Canonical Allele Identifier: CA5121121

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91775762C>T , CM000671.2:g.91775762C>T	GRCh38
NC_000009.11:g.94538044C>T , CM000671.1:g.94538044C>T	GRCh37
NC_000009.10:g.93577865C>T	NCBI36
NG_008089.1:g.179401G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.154G>A MANE Select	NP_004551.2:p.Gly52Ser
ENST00000375708.4:c.154G>A MANE Select	ENSP00000364860.3:p.Gly52Ser
NM_001318204.1:c.154G>A	NP_001305133.1:p.Gly52Ser
NM_001318204.2:c.154G>A	NP_001305133.1:p.Gly52Ser
NM_004560.3:c.154G>A	NP_004551.2:p.Gly52Ser
ENST00000375708.3:c.154G>A	ENSP00000364860.3:p.Gly52Ser
ENST00000375715.5:c.-267G>A	ENSP00000364867.1:n.-267G>A
ENST00000495386.5:n.417G>A
ENST00000546883.1:n.356G>A
ENST00000548585.2:n.20G>A
ENST00000550066.5:n.622G>A
XM_005252008.3:c.-267G>A	XP_005252065.1:n.-267G>A
XM_005252008.4:c.-267G>A	XP_005252065.1:n.-267G>A
XM_006717121.2:c.-267G>A	XP_006717184.1:n.-267G>A
XM_006717121.3:c.-267G>A	XP_006717184.1:n.-267G>A
XM_011518721.1:c.-267G>A	XP_011517023.1:n.-267G>A
XM_017014762.1:c.145G>A	XP_016870251.1:p.Gly49Ser
XM_017014763.1:c.-267G>A	XP_016870252.1:n.-267G>A
XR_001746315.1:n.397G>A