Canonical Allele Identifier: CA1668770995
Gene: ADGRG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.142370416G= , CM000668.2:g.142370416G= GRCh38
NC_000006.11:g.142691553G= , CM000668.1:g.142691553G= GRCh37
NC_000006.10:g.142733246G= NCBI36
NG_011839.1:g.73498G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296932.13:c.692G= ENSP00000296932.8:p.Cys231=
ENST00000367609.8:c.692G= MANE Select ENSP00000356581.3:p.Cys231=
ENST00000230173.10:c.692G= ENSP00000230173.6:p.Cys231=
ENST00000296932.12:c.692G= ENSP00000296932.8:p.Cys231=
ENST00000367608.6:c.692G= ENSP00000356580.2:p.Cys231=
ENST00000367609.7:c.692G= ENSP00000356581.3:p.Cys231=
ENST00000415128.6:n.1072G=
ENST00000541199.5:c.689G= ENSP00000446287.1:p.Cys230=
ENST00000545477.1:n.616+188G=
NM_001032394.2:c.692G= NP_001027566.1:p.Cys231=
NM_001032395.2:c.692G= NP_001027567.1:p.Cys231=
NM_020455.5:c.692G= NP_065188.4:p.Cys231=
NM_198569.2:c.692G= NP_940971.1:p.Cys231=
XM_005267061.2:c.695G= XP_005267118.1:p.Cys232=
XM_006715516.2:c.695G= XP_006715579.1:p.Cys232=
XM_006715517.2:c.689G= XP_006715580.1:p.Cys230=
XM_006715518.2:c.695G= XP_006715581.1:p.Cys232=
XM_011535964.1:c.692G= XP_011534266.1:p.Cys231=
XM_005267061.3:c.695G= XP_005267118.1:p.Cys232=
XM_017011085.1:c.695G= XP_016866574.1:p.Cys232=
NM_198569.3:c.692G= MANE Select NP_940971.2:p.Cys231=
NM_001032394.3:c.692G= NP_001027566.2:p.Cys231=
NM_001032395.3:c.692G= NP_001027567.2:p.Cys231=
NM_020455.6:c.692G= NP_065188.5:p.Cys231=