Canonical Allele Identifier: CA1863925719

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726698_91726724delinsGGGACCAAGATGTACAGAATCCCCATC , CM000671.2:g.91726698_91726724delinsGGGACCAAGATGTACAGAATCCCCATC	GRCh38
NC_000009.11:g.94488980_94489006delinsGGGACCAAGATGTACAGAATCCCCATC , CM000671.1:g.94488980_94489006delinsGGGACCAAGATGTACAGAATCCCCATC	GRCh37
NC_000009.10:g.93528801_93528827delinsGGGACCAAGATGTACAGAATCCCCATC	NCBI36
NG_008089.1:g.228439_228465delinsGATGGGGATTCTGTACATCTTGGTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1203_1229delinsGATGGGGATTCTGTACATCTTGGTCCC MANE Select	ENSP00000364860.3:p.Lys401=
ENST00000375708.3:c.1203_1229delinsGATGGGGATTCTGTACATCTTGGTCCC	ENSP00000364860.3:p.Lys401=
ENST00000375715.5:c.783_809delinsGATGGGGATTCTGTACATCTTGGTCCC	ENSP00000364867.1:p.Lys261=
ENST00000550066.5:n.1671_1697delinsGATGGGGATTCTGTACATCTTGGTCCC
NM_004560.3:c.1203_1229delinsGATGGGGATTCTGTACATCTTGGTCCC	NP_004551.2:p.Lys401=
XM_005252008.3:c.783_809delinsGATGGGGATTCTGTACATCTTGGTCCC	XP_005252065.1:p.Lys261=
XM_005252009.3:c.-1_26delinsGATGGGGATTCTGTACATCTTGGTCCC
XM_006717121.2:c.783_809delinsGATGGGGATTCTGTACATCTTGGTCCC	XP_006717184.1:p.Lys261=
XM_011518721.1:c.783_809delinsGATGGGGATTCTGTACATCTTGGTCCC	XP_011517023.1:p.Lys261=
NM_001318204.1:c.1169_1195delinsGATGGGGATTCTGTACATCTTGGTCCC	NP_001305133.1:p.Arg390=
XM_005252008.4:c.783_809delinsGATGGGGATTCTGTACATCTTGGTCCC	XP_005252065.1:p.Lys261=
XM_006717121.3:c.783_809delinsGATGGGGATTCTGTACATCTTGGTCCC	XP_006717184.1:p.Lys261=
XM_017014762.1:c.1194_1220delinsGATGGGGATTCTGTACATCTTGGTCCC	XP_016870251.1:p.Lys398=
XM_017014763.1:c.783_809delinsGATGGGGATTCTGTACATCTTGGTCCC	XP_016870252.1:p.Lys261=
XR_001746315.1:n.1412_1438delinsGATGGGGATTCTGTACATCTTGGTCCC
NM_004560.4:c.1203_1229delinsGATGGGGATTCTGTACATCTTGGTCCC MANE Select	NP_004551.2:p.Lys401=
NM_001318204.2:c.1169_1195delinsGATGGGGATTCTGTACATCTTGGTCCC	NP_001305133.1:p.Arg390=