Canonical Allele Identifier: CA1863923450

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757647_91757648delinsAG , CM000671.2:g.91757647_91757648delinsAG	GRCh38
NC_000009.11:g.94519929_94519930delinsAG , CM000671.1:g.94519929_94519930delinsAG	GRCh37
NC_000009.10:g.93559750_93559751delinsAG	NCBI36
NG_008089.1:g.197515_197516delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.176-89_176-88delinsCT MANE Select	ENSP00000364860.3:n.176-89_176-88delinsCT
ENST00000375708.3:c.176-89_176-88delinsCT	ENSP00000364860.3:n.176-89_176-88delinsCT
ENST00000375715.5:c.-245-89_-245-88delinsCT	ENSP00000364867.1:n.-245-89_-245-88delinsCT
ENST00000495386.5:n.439-89_439-88delinsCT
ENST00000546883.1:n.378-89_378-88delinsCT
ENST00000548585.2:n.42-89_42-88delinsCT
ENST00000550066.5:n.644-89_644-88delinsCT
NM_004560.3:c.176-89_176-88delinsCT	NP_004551.2:n.176-89_176-88delinsCT
XM_005252008.3:c.-245-89_-245-88delinsCT	XP_005252065.1:n.-245-89_-245-88delinsCT
XM_006717121.2:c.-245-89_-245-88delinsCT	XP_006717184.1:n.-245-89_-245-88delinsCT
XM_011518721.1:c.-245-89_-245-88delinsCT	XP_011517023.1:n.-245-89_-245-88delinsCT
NM_001318204.1:c.176-89_176-88delinsCT	NP_001305133.1:n.176-89_176-88delinsCT
XM_005252008.4:c.-245-89_-245-88delinsCT	XP_005252065.1:n.-245-89_-245-88delinsCT
XM_006717121.3:c.-245-89_-245-88delinsCT	XP_006717184.1:n.-245-89_-245-88delinsCT
XM_017014762.1:c.167-89_167-88delinsCT	XP_016870251.1:n.167-89_167-88delinsCT
XM_017014763.1:c.-245-89_-245-88delinsCT	XP_016870252.1:n.-245-89_-245-88delinsCT
XR_001746315.1:n.419-89_419-88delinsCT
NM_004560.4:c.176-89_176-88delinsCT MANE Select	NP_004551.2:n.176-89_176-88delinsCT
NM_001318204.2:c.176-89_176-88delinsCT	NP_001305133.1:n.176-89_176-88delinsCT