Canonical Allele Identifier: CA2834786662

Gene: ADGRG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142382944C>A , CM000668.2:g.142382944C>A	GRCh38
NC_000006.11:g.142704081C>A , CM000668.1:g.142704081C>A	GRCh37
NC_000006.10:g.142745774C>A	NCBI36
NG_011839.1:g.86026C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296932.13:c.1138+925C>A	ENSP00000296932.8:n.1138+925C>A
ENST00000367609.8:c.1139-816C>A MANE Select	ENSP00000356581.3:n.1139-816C>A
ENST00000230173.10:c.1139-816C>A	ENSP00000230173.6:n.1139-816C>A
ENST00000296932.12:c.1138+925C>A	ENSP00000296932.8:n.1138+925C>A
ENST00000367608.6:c.1138+925C>A	ENSP00000356580.2:n.1138+925C>A
ENST00000367609.7:c.1139-816C>A	ENSP00000356581.3:n.1139-816C>A
NM_001032394.2:c.1138+925C>A	NP_001027566.1:n.1138+925C>A
NM_001032395.2:c.1138+925C>A	NP_001027567.1:n.1138+925C>A
NM_020455.5:c.1139-816C>A	NP_065188.4:n.1139-816C>A
NM_198569.2:c.1139-816C>A	NP_940971.1:n.1139-816C>A
XM_005267061.2:c.1142-816C>A	XP_005267118.1:n.1142-816C>A
XM_006715516.2:c.1142-816C>A	XP_006715579.1:n.1142-816C>A
XM_006715517.2:c.1136-816C>A	XP_006715580.1:n.1136-816C>A
XM_006715518.2:c.1141+925C>A	XP_006715581.1:n.1141+925C>A
XM_011535964.1:c.1139-816C>A	XP_011534266.1:n.1139-816C>A
XM_005267061.3:c.1142-816C>A	XP_005267118.1:n.1142-816C>A
XM_017011085.1:c.1142-816C>A	XP_016866574.1:n.1142-816C>A
NM_198569.3:c.1139-816C>A MANE Select	NP_940971.2:n.1139-816C>A
NM_001032394.3:c.1138+925C>A	NP_001027566.2:n.1138+925C>A
NM_001032395.3:c.1138+925C>A	NP_001027567.2:n.1138+925C>A
NM_020455.6:c.1139-816C>A	NP_065188.5:n.1139-816C>A