Canonical Allele Identifier: CA1668803298
Gene: ADGRG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.142444203C= , CM000668.2:g.142444203C= GRCh38
NC_000006.11:g.142765340C= , CM000668.1:g.142765340C= GRCh37
NC_000006.10:g.142807033C= NCBI36
NG_011839.1:g.147285C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296932.13:c.*821C= ENSP00000296932.8:n.*821C=
ENST00000367609.8:c.*688C= MANE Select ENSP00000356581.3:n.*688C=
ENST00000230173.10:c.*821C= ENSP00000230173.6:n.*821C=
ENST00000296932.12:c.*821C= ENSP00000296932.8:n.*821C=
ENST00000367608.6:c.*688C= ENSP00000356580.2:n.*688C=
ENST00000367609.7:c.*688C= ENSP00000356581.3:n.*688C=
NM_001032394.2:c.*821C= NP_001027566.1:n.*821C=
NM_001032395.2:c.*688C= NP_001027567.1:n.*688C=
NM_020455.5:c.*821C= NP_065188.4:n.*821C=
NM_198569.2:c.*688C= NP_940971.1:n.*688C=
XM_005267061.2:c.*821C= XP_005267118.1:n.*821C=
XM_006715516.2:c.*688C= XP_006715579.1:n.*688C=
XM_006715517.2:c.*688C= XP_006715580.1:n.*688C=
XM_006715518.2:c.*688C= XP_006715581.1:n.*688C=
XM_011535964.1:c.*688C= XP_011534266.1:n.*688C=
XM_005267061.3:c.*821C= XP_005267118.1:n.*821C=
NM_198569.3:c.*688C= MANE Select NP_940971.2:n.*688C=
NM_001032394.3:c.*821C= NP_001027566.2:n.*821C=
NM_001032395.3:c.*688C= NP_001027567.2:n.*688C=
NM_020455.6:c.*821C= NP_065188.5:n.*821C=