Canonical Allele Identifier: CA5120453

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724279A>G , CM000671.2:g.91724279A>G	GRCh38
NC_000009.11:g.94486561A>G , CM000671.1:g.94486561A>G	GRCh37
NC_000009.10:g.93526382A>G	NCBI36
NG_008089.1:g.230884T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.2215T>C MANE Select	NP_004551.2:p.Phe739Leu
ENST00000375708.4:c.2215T>C MANE Select	ENSP00000364860.3:p.Phe739Leu
NM_004560.3:c.2215T>C	NP_004551.2:p.Phe739Leu
ENST00000375708.3:c.2215T>C	ENSP00000364860.3:p.Phe739Leu
ENST00000375715.5:c.1795T>C	ENSP00000364867.1:p.Phe599Leu
ENST00000550066.5:n.2683T>C
XM_005252008.3:c.1795T>C	XP_005252065.1:p.Phe599Leu
XM_005252008.4:c.1795T>C	XP_005252065.1:p.Phe599Leu
XM_005252009.3:c.1012T>C	XP_005252066.1:p.Phe338Leu
XM_006717121.2:c.1795T>C	XP_006717184.1:p.Phe599Leu
XM_006717121.3:c.1795T>C	XP_006717184.1:p.Phe599Leu
XM_011518721.1:c.1795T>C	XP_011517023.1:p.Phe599Leu
XM_017014762.1:c.2206T>C	XP_016870251.1:p.Phe736Leu
XM_017014763.1:c.1795T>C	XP_016870252.1:p.Phe599Leu