Canonical Allele Identifier: CA2970214831

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91871120G>A , CM000671.2:g.91871120G>A	GRCh38
NC_000009.11:g.94633402G>A , CM000671.1:g.94633402G>A	GRCh37
NC_000009.10:g.93673223G>A	NCBI36
NG_008089.1:g.84043C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.97+78747C>T MANE Select	NP_004551.2:n.97+78747C>T
ENST00000375708.4:c.97+78747C>T MANE Select	ENSP00000364860.3:n.97+78747C>T
NM_001318204.1:c.97+78747C>T	NP_001305133.1:n.97+78747C>T
NM_001318204.2:c.97+78747C>T	NP_001305133.1:n.97+78747C>T
NM_004560.3:c.97+78747C>T	NP_004551.2:n.97+78747C>T
ENST00000375708.3:c.97+78747C>T	ENSP00000364860.3:n.97+78747C>T
ENST00000375715.5:c.-324+77487C>T	ENSP00000364867.1:n.-324+77487C>T
ENST00000495386.5:n.360+12138C>T
ENST00000546883.1:n.299+52645C>T
ENST00000550066.5:n.565+12138C>T
XM_005252008.3:c.-324+77487C>T	XP_005252065.1:n.-324+77487C>T
XM_005252008.4:c.-324+77487C>T	XP_005252065.1:n.-324+77487C>T
XM_011518721.1:c.-324+12138C>T	XP_011517023.1:n.-324+12138C>T
XM_017014763.1:c.-324+78438C>T	XP_016870252.1:n.-324+78438C>T
XR_001746315.1:n.340+78747C>T
XR_001746831.1:n.1262+12138C>T
XR_001746832.1:n.1262+12138C>T
XR_001746833.1:n.1169+12138C>T