Canonical Allele Identifier: CA6541312

Gene: ADCY6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48776526G>A , CM000674.2:g.48776526G>A	GRCh38
NC_000012.11:g.49170309G>A , CM000674.1:g.49170309G>A	GRCh37
NC_000012.10:g.47456576G>A	NCBI36
NG_042166.1:g.17571C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357869.8:c.1437C>T MANE Select	ENSP00000350536.4:p.Arg479=
ENST00000307885.4:c.1437C>T	ENSP00000311405.4:p.Arg479=
ENST00000357869.7:c.1437C>T	ENSP00000350536.3:p.Arg479=
ENST00000550422.5:c.1437C>T	ENSP00000446730.1:p.Arg479=
ENST00000551435.1:n.679C>T
NM_015270.3:c.1437C>T	NP_056085.1:p.Arg479=
NM_015270.4:c.1437C>T	NP_056085.1:p.Arg479=
NM_020983.2:c.1437C>T	NP_066193.1:p.Arg479=
XM_006719210.2:c.1437C>T	XP_006719273.1:p.Arg479=
XM_011537810.1:c.1437C>T	XP_011536112.1:p.Arg479=
XM_011537811.1:c.1437C>T	XP_011536113.1:p.Arg479=
XM_011537812.1:c.1437C>T	XP_011536114.1:p.Arg479=
XM_011537813.1:c.1437C>T	XP_011536115.1:p.Arg479=
XR_944483.1:n.1479C>T
XM_006719210.4:c.1437C>T	XP_006719273.1:p.Arg479=
XM_017018743.1:c.1437C>T	XP_016874232.1:p.Arg479=
XR_001748565.1:n.1437C>T
NM_015270.5:c.1437C>T MANE Select	NP_056085.1:p.Arg479=
NM_001390830.1:c.1437C>T	NP_001377759.1:p.Arg479=
NM_001390831.1:c.1437C>T	NP_001377760.1:p.Arg479=