Canonical Allele Identifier: CA1668770960

Gene: ADGRG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142370325G= , CM000668.2:g.142370325G=	GRCh38
NC_000006.11:g.142691462G= , CM000668.1:g.142691462G=	GRCh37
NC_000006.10:g.142733155G=	NCBI36
NG_011839.1:g.73407G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296932.13:c.601G=	ENSP00000296932.8:p.Ala201=
ENST00000367609.8:c.601G= MANE Select	ENSP00000356581.3:p.Ala201=
ENST00000230173.10:c.601G=	ENSP00000230173.6:p.Ala201=
ENST00000296932.12:c.601G=	ENSP00000296932.8:p.Ala201=
ENST00000367608.6:c.601G=	ENSP00000356580.2:p.Ala201=
ENST00000367609.7:c.601G=	ENSP00000356581.3:p.Ala201=
ENST00000415128.6:n.981G=
ENST00000541199.5:c.598G=	ENSP00000446287.1:p.Ala200=
ENST00000545477.1:n.616+97G=
NM_001032394.2:c.601G=	NP_001027566.1:p.Ala201=
NM_001032395.2:c.601G=	NP_001027567.1:p.Ala201=
NM_020455.5:c.601G=	NP_065188.4:p.Ala201=
NM_198569.2:c.601G=	NP_940971.1:p.Ala201=
XM_005267061.2:c.604G=	XP_005267118.1:p.Ala202=
XM_006715516.2:c.604G=	XP_006715579.1:p.Ala202=
XM_006715517.2:c.598G=	XP_006715580.1:p.Ala200=
XM_006715518.2:c.604G=	XP_006715581.1:p.Ala202=
XM_011535964.1:c.601G=	XP_011534266.1:p.Ala201=
XM_005267061.3:c.604G=	XP_005267118.1:p.Ala202=
XM_017011085.1:c.604G=	XP_016866574.1:p.Ala202=
NM_198569.3:c.601G= MANE Select	NP_940971.2:p.Ala201=
NM_001032394.3:c.601G=	NP_001027566.2:p.Ala201=
NM_001032395.3:c.601G=	NP_001027567.2:p.Ala201=
NM_020455.6:c.601G=	NP_065188.5:p.Ala201=