Canonical Allele Identifier: CA452650049

Gene: ADGRG6

Linked Data

• MyVariant Identifiers: chr6:g.142691575T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142370438T>A , CM000668.2:g.142370438T>A	GRCh38
NC_000006.11:g.142691575T>A , CM000668.1:g.142691575T>A	GRCh37
NC_000006.10:g.142733268T>A	NCBI36
NG_011839.1:g.73520T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296932.13:c.714T>A	ENSP00000296932.8:p.Pro238=
ENST00000367609.8:c.714T>A MANE Select	ENSP00000356581.3:p.Pro238=
ENST00000230173.10:c.714T>A	ENSP00000230173.6:p.Pro238=
ENST00000296932.12:c.714T>A	ENSP00000296932.8:p.Pro238=
ENST00000367608.6:c.714T>A	ENSP00000356580.2:p.Pro238=
ENST00000367609.7:c.714T>A	ENSP00000356581.3:p.Pro238=
ENST00000415128.6:n.1094T>A
ENST00000541199.5:c.711T>A	ENSP00000446287.1:p.Pro237=
ENST00000545477.1:n.616+210T>A
NM_001032394.2:c.714T>A	NP_001027566.1:p.Pro238=
NM_001032395.2:c.714T>A	NP_001027567.1:p.Pro238=
NM_020455.5:c.714T>A	NP_065188.4:p.Pro238=
NM_198569.2:c.714T>A	NP_940971.1:p.Pro238=
XM_005267061.2:c.717T>A	XP_005267118.1:p.Pro239=
XM_006715516.2:c.717T>A	XP_006715579.1:p.Pro239=
XM_006715517.2:c.711T>A	XP_006715580.1:p.Pro237=
XM_006715518.2:c.717T>A	XP_006715581.1:p.Pro239=
XM_011535964.1:c.714T>A	XP_011534266.1:p.Pro238=
XM_005267061.3:c.717T>A	XP_005267118.1:p.Pro239=
XM_017011085.1:c.717T>A	XP_016866574.1:p.Pro239=
NM_198569.3:c.714T>A MANE Select	NP_940971.2:p.Pro238=
NM_001032394.3:c.714T>A	NP_001027566.2:p.Pro238=
NM_001032395.3:c.714T>A	NP_001027567.2:p.Pro238=
NM_020455.6:c.714T>A	NP_065188.5:p.Pro238=