Canonical Allele Identifier: CA373801228

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91733342G>T , CM000671.2:g.91733342G>T	GRCh38
NC_000009.11:g.94495624G>T , CM000671.1:g.94495624G>T	GRCh37
NC_000009.10:g.93535445G>T	NCBI36
NG_008089.1:g.221821C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.717C>A MANE Select	NP_004551.2:p.Cys239Ter
ENST00000375708.4:c.717C>A MANE Select	ENSP00000364860.3:p.Cys239Ter
NM_001318204.1:c.717C>A	NP_001305133.1:p.Cys239Ter
NM_001318204.2:c.717C>A	NP_001305133.1:p.Cys239Ter
NM_004560.3:c.717C>A	NP_004551.2:p.Cys239Ter
ENST00000375708.3:c.717C>A	ENSP00000364860.3:p.Cys239Ter
ENST00000375715.5:c.297C>A	ENSP00000364867.1:p.Cys99Ter
ENST00000550066.5:n.1185C>A
XM_005252008.3:c.297C>A	XP_005252065.1:p.Cys99Ter
XM_005252008.4:c.297C>A	XP_005252065.1:p.Cys99Ter
XM_006717121.2:c.297C>A	XP_006717184.1:p.Cys99Ter
XM_006717121.3:c.297C>A	XP_006717184.1:p.Cys99Ter
XM_011518721.1:c.297C>A	XP_011517023.1:p.Cys99Ter
XM_017014762.1:c.708C>A	XP_016870251.1:p.Cys236Ter
XM_017014763.1:c.297C>A	XP_016870252.1:p.Cys99Ter
XR_001746315.1:n.960C>A