Canonical Allele Identifier: CA1668803310
Gene: ADGRG6 HGNC NCBI

Linked Data

dbSNP Id: rs1777884862

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.142444233_142444236del , CM000668.2:g.142444233_142444236del GRCh38
NC_000006.11:g.142765370_142765373del , CM000668.1:g.142765370_142765373del GRCh37
NC_000006.10:g.142807063_142807066del NCBI36
NG_011839.1:g.147315_147318del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296932.13:c.*851_*854del ENSP00000296932.8:n.*851_*854del
ENST00000367609.8:c.*718_*721del MANE Select ENSP00000356581.3:n.*718_*721del
ENST00000230173.10:c.*851_*854del ENSP00000230173.6:n.*851_*854del
ENST00000296932.12:c.*851_*854del ENSP00000296932.8:n.*851_*854del
ENST00000367608.6:c.*718_*721del ENSP00000356580.2:n.*718_*721del
ENST00000367609.7:c.*718_*721del ENSP00000356581.3:n.*718_*721del
NM_001032394.2:c.*851_*854del NP_001027566.1:n.*851_*854del
NM_001032395.2:c.*718_*721del NP_001027567.1:n.*718_*721del
NM_020455.5:c.*851_*854del NP_065188.4:n.*851_*854del
NM_198569.2:c.*718_*721del NP_940971.1:n.*718_*721del
XM_005267061.2:c.*851_*854del XP_005267118.1:n.*851_*854del
XM_006715516.2:c.*718_*721del XP_006715579.1:n.*718_*721del
XM_006715517.2:c.*718_*721del XP_006715580.1:n.*718_*721del
XM_006715518.2:c.*718_*721del XP_006715581.1:n.*718_*721del
XM_011535964.1:c.*718_*721del XP_011534266.1:n.*718_*721del
XM_005267061.3:c.*851_*854del XP_005267118.1:n.*851_*854del
NM_198569.3:c.*718_*721del MANE Select NP_940971.2:n.*718_*721del
NM_001032394.3:c.*851_*854del NP_001027566.2:n.*851_*854del
NM_001032395.3:c.*718_*721del NP_001027567.2:n.*718_*721del
NM_020455.6:c.*851_*854del NP_065188.5:n.*851_*854del