Canonical Allele Identifier: CA1863921530

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723766G= , CM000671.2:g.91723766G=	GRCh38
NC_000009.11:g.94486048G= , CM000671.1:g.94486048G=	GRCh37
NC_000009.10:g.93525869G=	NCBI36
NG_008089.1:g.231397C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2728C= MANE Select	ENSP00000364860.3:p.Gln910=
ENST00000375708.3:c.2728C=	ENSP00000364860.3:p.Gln910=
ENST00000375715.5:c.1920+388C=	ENSP00000364867.1:n.1920+388C=
ENST00000550066.5:n.3196C=
NM_004560.3:c.2728C=	NP_004551.2:p.Gln910=
XM_005252008.3:c.2308C=	XP_005252065.1:p.Gln770=
XM_005252009.3:c.1525C=	XP_005252066.1:p.Gln509=
XM_006717121.2:c.2308C=	XP_006717184.1:p.Gln770=
XM_011518721.1:c.2308C=	XP_011517023.1:p.Gln770=
XM_005252008.4:c.2308C=	XP_005252065.1:p.Gln770=
XM_006717121.3:c.2308C=	XP_006717184.1:p.Gln770=
XM_017014762.1:c.2719C=	XP_016870251.1:p.Gln907=
XM_017014763.1:c.2308C=	XP_016870252.1:p.Gln770=
NM_004560.4:c.2728C= MANE Select	NP_004551.2:p.Gln910=