Canonical Allele Identifier: CA2838243560
Gene: ADCY6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48774855C>A , CM000674.2:g.48774855C>A GRCh38
NC_000012.11:g.49168638C>A , CM000674.1:g.49168638C>A GRCh37
NC_000012.10:g.47454905C>A NCBI36
NG_042166.1:g.19242G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357869.8:c.2079-77G>T MANE Select ENSP00000350536.4:n.2079-77G>T
ENST00000307885.4:c.2079-77G>T ENSP00000311405.4:n.2079-77G>T
ENST00000357869.7:c.2079-77G>T ENSP00000350536.3:n.2079-77G>T
ENST00000550422.5:c.2079-77G>T ENSP00000446730.1:n.2079-77G>T
ENST00000552090.1:n.600+102G>T
NM_015270.3:c.2079-77G>T NP_056085.1:n.2079-77G>T
NM_015270.4:c.2079-77G>T NP_056085.1:n.2079-77G>T
NM_020983.2:c.2079-77G>T NP_066193.1:n.2079-77G>T
XM_006719210.2:c.2079-77G>T XP_006719273.1:n.2079-77G>T
XM_011537810.1:c.1980+448G>T XP_011536112.1:n.1980+448G>T
XM_011537811.1:c.1980+448G>T XP_011536113.1:n.1980+448G>T
XM_011537812.1:c.2079-77G>T XP_011536114.1:n.2079-77G>T
XM_011537813.1:c.2079-77G>T XP_011536115.1:n.2079-77G>T
XR_944483.1:n.2121-77G>T
XM_006719210.4:c.2079-77G>T XP_006719273.1:n.2079-77G>T
XM_017018743.1:c.1980+448G>T XP_016874232.1:n.1980+448G>T
XR_001748565.1:n.2079-77G>T
NM_015270.5:c.2079-77G>T MANE Select NP_056085.1:n.2079-77G>T
NM_001390830.1:c.2079-77G>T NP_001377759.1:n.2079-77G>T
NM_001390831.1:c.2079-77G>T NP_001377760.1:n.2079-77G>T