Canonical Allele Identifier: CA12395490
Gene: ADGRG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.142334664T>A , CM000668.2:g.142334664T>A GRCh38
NC_000006.11:g.142655801T>A , CM000668.1:g.142655801T>A GRCh37
NC_000006.10:g.142697494T>A NCBI36
NG_011839.1:g.37746T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296932.13:c.103+25020T>A ENSP00000296932.8:n.103+25020T>A
ENST00000367609.8:c.103+25020T>A MANE Select ENSP00000356581.3:n.103+25020T>A
ENST00000230173.10:c.103+25020T>A ENSP00000230173.6:n.103+25020T>A
ENST00000296932.12:c.103+25020T>A ENSP00000296932.8:n.103+25020T>A
ENST00000367608.6:c.103+25020T>A ENSP00000356580.2:n.103+25020T>A
ENST00000367609.7:c.103+25020T>A ENSP00000356581.3:n.103+25020T>A
ENST00000415128.6:n.483+25020T>A
ENST00000435011.6:c.100+25020T>A ENSP00000438366.1:n.100+25020T>A
ENST00000541199.5:c.100+25020T>A ENSP00000446287.1:n.100+25020T>A
ENST00000545477.1:n.215+25020T>A
NM_001032394.2:c.103+25020T>A NP_001027566.1:n.103+25020T>A
NM_001032395.2:c.103+25020T>A NP_001027567.1:n.103+25020T>A
NM_020455.5:c.103+25020T>A NP_065188.4:n.103+25020T>A
NM_198569.2:c.103+25020T>A NP_940971.1:n.103+25020T>A
XM_005267061.2:c.103+25020T>A XP_005267118.1:n.103+25020T>A
XM_006715516.2:c.103+25020T>A XP_006715579.1:n.103+25020T>A
XM_006715517.2:c.100+25020T>A XP_006715580.1:n.100+25020T>A
XM_006715518.2:c.103+25020T>A XP_006715581.1:n.103+25020T>A
XM_011535964.1:c.100+25020T>A XP_011534266.1:n.100+25020T>A
XM_005267061.3:c.103+25020T>A XP_005267118.1:n.103+25020T>A
XM_017011085.1:c.103+25020T>A XP_016866574.1:n.103+25020T>A
NM_198569.3:c.103+25020T>A MANE Select NP_940971.2:n.103+25020T>A
NM_001032394.3:c.103+25020T>A NP_001027566.2:n.103+25020T>A
NM_001032395.3:c.103+25020T>A NP_001027567.2:n.103+25020T>A
NM_020455.6:c.103+25020T>A NP_065188.5:n.103+25020T>A