Canonical Allele Identifier: CA16582160
Gene: RALY HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2284378

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34000289T>C , CM000682.2:g.34000289T>C GRCh38
NC_000020.10:g.32588095T>C , CM000682.1:g.32588095T>C GRCh37
NC_000020.9:g.32051756T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_007367.3:c.-93+6158T>C VV NP_031393.2:p.=
NM_016732.2:c.-93+6158T>C VV NP_057951.1:p.=
XM_005260334.3:c.-10+6158T>C XP_005260391.1:p.=
XM_005260336.3:c.-10+6158T>C XP_005260393.1:p.=
XM_011528695.1:c.-210+6158T>C XP_011526997.1:p.=
XM_005260334.5:c.-10+6158T>C XP_005260391.1:p.=
XM_005260336.5:c.-10+6158T>C XP_005260393.1:p.=
XM_011528695.3:c.-210+6158T>C XP_011526997.1:p.=
XM_017027731.2:c.-10+6158T>C XP_016883220.1:p.=
XM_024451859.1:c.-93+6158T>C XP_024307627.1:p.=
NM_016732.3:c.-93+6158T>C VV MANE Preferred NP_057951.1:p.=
ENST00000246194.7:c.-93+6158T>C ENSP00000246194.3:p.=
ENST00000333552.9:c.-93+6158T>C ENSP00000327522.5:p.=
ENST00000375114.7:c.-93+6158T>C ENSP00000364255.3:p.=
ENST00000413297.5:c.-169+6158T>C ENSP00000403744.1:p.=
ENST00000448364.5:c.-210+6158T>C ENSP00000413638.1:p.=