Canonical Allele Identifier: CA2539958151

Gene: ADGRG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142444293A>G , CM000668.2:g.142444293A>G	GRCh38
NC_000006.11:g.142765430A>G , CM000668.1:g.142765430A>G	GRCh37
NC_000006.10:g.142807123A>G	NCBI36
NG_011839.1:g.147375A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296932.13:c.*911A>G	ENSP00000296932.8:n.*911A>G
ENST00000367609.8:c.*778A>G MANE Select	ENSP00000356581.3:n.*778A>G
ENST00000230173.10:c.*911A>G	ENSP00000230173.6:n.*911A>G
ENST00000296932.12:c.*911A>G	ENSP00000296932.8:n.*911A>G
ENST00000367608.6:c.*778A>G	ENSP00000356580.2:n.*778A>G
ENST00000367609.7:c.*778A>G	ENSP00000356581.3:n.*778A>G
NM_001032394.2:c.*911A>G	NP_001027566.1:n.*911A>G
NM_001032395.2:c.*778A>G	NP_001027567.1:n.*778A>G
NM_020455.5:c.*911A>G	NP_065188.4:n.*911A>G
NM_198569.2:c.*778A>G	NP_940971.1:n.*778A>G
XM_005267061.2:c.*911A>G	XP_005267118.1:n.*911A>G
XM_006715516.2:c.*778A>G	XP_006715579.1:n.*778A>G
XM_006715517.2:c.*778A>G	XP_006715580.1:n.*778A>G
XM_006715518.2:c.*778A>G	XP_006715581.1:n.*778A>G
XM_011535964.1:c.*778A>G	XP_011534266.1:n.*778A>G
XM_005267061.3:c.*911A>G	XP_005267118.1:n.*911A>G
NM_198569.3:c.*778A>G MANE Select	NP_940971.2:n.*778A>G
NM_001032394.3:c.*911A>G	NP_001027566.2:n.*911A>G
NM_001032395.3:c.*778A>G	NP_001027567.2:n.*778A>G
NM_020455.6:c.*911A>G	NP_065188.5:n.*911A>G