Canonical Allele Identifier: CA4026697

Gene: ADGRG6

Linked Data

• dbSNP Id: rs754502589
• ExAC: 6:142691553 G / A
• gnomAD v2: 6-142691553-G-A
• gnomAD v4: 6-142370416-G-A
• MyVariant Identifiers: chr6:g.142691553G>A (hg19) ; chr6:g.142370416G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142370416G>A , CM000668.2:g.142370416G>A	GRCh38
NC_000006.11:g.142691553G>A , CM000668.1:g.142691553G>A	GRCh37
NC_000006.10:g.142733246G>A	NCBI36
NG_011839.1:g.73498G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000296932.13:c.692G>A	ENSP00000296932.8:p.Cys231Tyr
ENST00000367609.8:c.692G>A MANE Select	ENSP00000356581.3:p.Cys231Tyr
ENST00000230173.10:c.692G>A	ENSP00000230173.6:p.Cys231Tyr
ENST00000296932.12:c.692G>A	ENSP00000296932.8:p.Cys231Tyr
ENST00000367608.6:c.692G>A	ENSP00000356580.2:p.Cys231Tyr
ENST00000367609.7:c.692G>A	ENSP00000356581.3:p.Cys231Tyr
ENST00000415128.6:n.1072G>A
ENST00000541199.5:c.689G>A	ENSP00000446287.1:p.Cys230Tyr
ENST00000545477.1:n.616+188G>A
NM_001032394.2:c.692G>A	NP_001027566.1:p.Cys231Tyr
NM_001032395.2:c.692G>A	NP_001027567.1:p.Cys231Tyr
NM_020455.5:c.692G>A	NP_065188.4:p.Cys231Tyr
NM_198569.2:c.692G>A	NP_940971.1:p.Cys231Tyr
XM_005267061.2:c.695G>A	XP_005267118.1:p.Cys232Tyr
XM_006715516.2:c.695G>A	XP_006715579.1:p.Cys232Tyr
XM_006715517.2:c.689G>A	XP_006715580.1:p.Cys230Tyr
XM_006715518.2:c.695G>A	XP_006715581.1:p.Cys232Tyr
XM_011535964.1:c.692G>A	XP_011534266.1:p.Cys231Tyr
XM_005267061.3:c.695G>A	XP_005267118.1:p.Cys232Tyr
XM_017011085.1:c.695G>A	XP_016866574.1:p.Cys232Tyr
NM_198569.3:c.692G>A MANE Select	NP_940971.2:p.Cys231Tyr
NM_001032394.3:c.692G>A	NP_001027566.2:p.Cys231Tyr
NM_001032395.3:c.692G>A	NP_001027567.2:p.Cys231Tyr
NM_020455.6:c.692G>A	NP_065188.5:p.Cys231Tyr