Canonical Allele Identifier: CA452649900

Gene: ADGRG6

Linked Data

• MyVariant Identifiers: chr6:g.142691449C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142370312C>T , CM000668.2:g.142370312C>T	GRCh38
NC_000006.11:g.142691449C>T , CM000668.1:g.142691449C>T	GRCh37
NC_000006.10:g.142733142C>T	NCBI36
NG_011839.1:g.73394C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000296932.13:c.588C>T	ENSP00000296932.8:p.Asp196=
ENST00000367609.8:c.588C>T MANE Select	ENSP00000356581.3:p.Asp196=
ENST00000230173.10:c.588C>T	ENSP00000230173.6:p.Asp196=
ENST00000296932.12:c.588C>T	ENSP00000296932.8:p.Asp196=
ENST00000367608.6:c.588C>T	ENSP00000356580.2:p.Asp196=
ENST00000367609.7:c.588C>T	ENSP00000356581.3:p.Asp196=
ENST00000415128.6:n.968C>T
ENST00000541199.5:c.585C>T	ENSP00000446287.1:p.Asp195=
ENST00000545477.1:n.616+84C>T
NM_001032394.2:c.588C>T	NP_001027566.1:p.Asp196=
NM_001032395.2:c.588C>T	NP_001027567.1:p.Asp196=
NM_020455.5:c.588C>T	NP_065188.4:p.Asp196=
NM_198569.2:c.588C>T	NP_940971.1:p.Asp196=
XM_005267061.2:c.591C>T	XP_005267118.1:p.Asp197=
XM_006715516.2:c.591C>T	XP_006715579.1:p.Asp197=
XM_006715517.2:c.585C>T	XP_006715580.1:p.Asp195=
XM_006715518.2:c.591C>T	XP_006715581.1:p.Asp197=
XM_011535964.1:c.588C>T	XP_011534266.1:p.Asp196=
XM_005267061.3:c.591C>T	XP_005267118.1:p.Asp197=
XM_017011085.1:c.591C>T	XP_016866574.1:p.Asp197=
NM_198569.3:c.588C>T MANE Select	NP_940971.2:p.Asp196=
NM_001032394.3:c.588C>T	NP_001027566.2:p.Asp196=
NM_001032395.3:c.588C>T	NP_001027567.2:p.Asp196=
NM_020455.6:c.588C>T	NP_065188.5:p.Asp196=