Canonical Allele Identifier: CA1668739497

Gene: ADGRG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142302104T>C , CM000668.2:g.142302104T>C	GRCh38
NC_000006.11:g.142623241T>C , CM000668.1:g.142623241T>C	GRCh37
NC_000006.10:g.142664934T>C	NCBI36
NG_011839.1:g.5186T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_198569.3:c.-226T>C MANE Select	NP_940971.2:n.-226T>C
ENST00000367609.8:c.-226T>C MANE Select	ENSP00000356581.3:n.-226T>C
NM_001032394.2:c.-226T>C	NP_001027566.1:n.-226T>C
NM_001032394.3:c.-226T>C	NP_001027566.2:n.-226T>C
NM_001032395.2:c.-226T>C	NP_001027567.1:n.-226T>C
NM_001032395.3:c.-226T>C	NP_001027567.2:n.-226T>C
NM_020455.5:c.-226T>C	NP_065188.4:n.-226T>C
NM_020455.6:c.-226T>C	NP_065188.5:n.-226T>C
NM_198569.2:c.-226T>C	NP_940971.1:n.-226T>C
ENST00000230173.10:c.-226T>C	ENSP00000230173.6:n.-226T>C
ENST00000296932.12:c.-226T>C	ENSP00000296932.8:n.-226T>C
ENST00000296932.13:c.-226T>C	ENSP00000296932.8:n.-226T>C
ENST00000367608.6:c.-226T>C	ENSP00000356580.2:n.-226T>C
ENST00000367609.7:c.-226T>C	ENSP00000356581.3:n.-226T>C
ENST00000415128.6:n.155T>C
XM_005267061.2:c.-226T>C	XP_005267118.1:n.-226T>C
XM_005267061.3:c.-226T>C	XP_005267118.1:n.-226T>C
XM_006715516.2:c.-226T>C	XP_006715579.1:n.-226T>C
XM_006715518.2:c.-226T>C	XP_006715581.1:n.-226T>C
XM_017011085.1:c.-226T>C	XP_016866574.1:n.-226T>C