Canonical Allele Identifier: CA868430532

Gene: ROR2

Linked Data

• dbSNP Id: rs1197533608
• MyVariant Identifiers: chr9:g.94486331del (hg19) ; chr9:g.91724049del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724049del , CM000671.2:g.91724049del	GRCh38
NC_000009.11:g.94486331del , CM000671.1:g.94486331del	GRCh37
NC_000009.10:g.93526152del	NCBI36
NG_008089.1:g.231114del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2445del MANE Select	ENSP00000364860.3:p.Gln816SerfsTer?
ENST00000375708.3:c.2445del	ENSP00000364860.3:p.Gln816SerfsTer?
ENST00000375715.5:c.1920+105del	ENSP00000364867.1:n.1920+105del
ENST00000550066.5:n.2913del
NM_004560.3:c.2445del	NP_004551.2:p.Gln816SerfsTer?
XM_005252008.3:c.2025del	XP_005252065.1:p.Gln676SerfsTer?
XM_005252009.3:c.1242del	XP_005252066.1:p.Gln415SerfsTer?
XM_006717121.2:c.2025del	XP_006717184.1:p.Gln676SerfsTer?
XM_011518721.1:c.2025del	XP_011517023.1:p.Gln676SerfsTer?
XM_005252008.4:c.2025del	XP_005252065.1:p.Gln676SerfsTer?
XM_006717121.3:c.2025del	XP_006717184.1:p.Gln676SerfsTer?
XM_017014762.1:c.2436del	XP_016870251.1:p.Gln813SerfsTer?
XM_017014763.1:c.2025del	XP_016870252.1:p.Gln676SerfsTer?
NM_004560.4:c.2445del MANE Select	NP_004551.2:p.Gln816SerfsTer?