Canonical Allele Identifier: CA5120905

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91733315C>T , CM000671.2:g.91733315C>T	GRCh38
NC_000009.11:g.94495597C>T , CM000671.1:g.94495597C>T	GRCh37
NC_000009.10:g.93535418C>T	NCBI36
NG_008089.1:g.221848G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.744G>A MANE Select	ENSP00000364860.3:p.Pro248=
ENST00000375708.3:c.744G>A	ENSP00000364860.3:p.Pro248=
ENST00000375715.5:c.324G>A	ENSP00000364867.1:p.Pro108=
ENST00000550066.5:n.1212G>A
NM_004560.3:c.744G>A	NP_004551.2:p.Pro248=
XM_005252008.3:c.324G>A	XP_005252065.1:p.Pro108=
XM_006717121.2:c.324G>A	XP_006717184.1:p.Pro108=
XM_011518721.1:c.324G>A	XP_011517023.1:p.Pro108=
NM_001318204.1:c.744G>A	NP_001305133.1:p.Pro248=
XM_005252008.4:c.324G>A	XP_005252065.1:p.Pro108=
XM_006717121.3:c.324G>A	XP_006717184.1:p.Pro108=
XM_017014762.1:c.735G>A	XP_016870251.1:p.Pro245=
XM_017014763.1:c.324G>A	XP_016870252.1:p.Pro108=
XR_001746315.1:n.987G>A
NM_004560.4:c.744G>A MANE Select	NP_004551.2:p.Pro248=
NM_001318204.2:c.744G>A	NP_001305133.1:p.Pro248=