Canonical Allele Identifier: CA373799828

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726738G>A , CM000671.2:g.91726738G>A	GRCh38
NC_000009.11:g.94489020G>A , CM000671.1:g.94489020G>A	GRCh37
NC_000009.10:g.93528841G>A	NCBI36
NG_008089.1:g.228425C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.1189C>T MANE Select	NP_004551.2:p.Arg397Ter
ENST00000375708.4:c.1189C>T MANE Select	ENSP00000364860.3:p.Arg397Ter
NM_001318204.1:c.1155C>T	NP_001305133.1:p.Pro385=
NM_001318204.2:c.1155C>T	NP_001305133.1:p.Pro385=
NM_004560.3:c.1189C>T	NP_004551.2:p.Arg397Ter
ENST00000375708.3:c.1189C>T	ENSP00000364860.3:p.Arg397Ter
ENST00000375715.5:c.769C>T	ENSP00000364867.1:p.Arg257Ter
ENST00000550066.5:n.1657C>T
XM_005252008.3:c.769C>T	XP_005252065.1:p.Arg257Ter
XM_005252008.4:c.769C>T	XP_005252065.1:p.Arg257Ter
XM_005252009.3:c.-15C>T	XP_005252066.1:n.-15C>T
XM_006717121.2:c.769C>T	XP_006717184.1:p.Arg257Ter
XM_006717121.3:c.769C>T	XP_006717184.1:p.Arg257Ter
XM_011518721.1:c.769C>T	XP_011517023.1:p.Arg257Ter
XM_017014762.1:c.1180C>T	XP_016870251.1:p.Arg394Ter
XM_017014763.1:c.769C>T	XP_016870252.1:p.Arg257Ter
XR_001746315.1:n.1398C>T