Canonical Allele Identifier: CA236595128

Gene: ADCY6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48770699G>A , CM000674.2:g.48770699G>A	GRCh38
NC_000012.11:g.49164482G>A , CM000674.1:g.49164482G>A	GRCh37
NC_000012.10:g.47450749G>A	NCBI36
NG_042166.1:g.23398C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357869.8:c.3256+67C>T MANE Select	ENSP00000350536.4:n.3256+67C>T
ENST00000307885.4:c.3256+67C>T	ENSP00000311405.4:n.3256+67C>T
ENST00000357869.7:c.3097+67C>T	ENSP00000350536.3:n.3097+67C>T
ENST00000547260.5:n.2110+67C>T
ENST00000550422.5:c.3097+67C>T	ENSP00000446730.1:n.3097+67C>T
NM_015270.3:c.3256+67C>T	NP_056085.1:n.3256+67C>T
NM_015270.4:c.3256+67C>T	NP_056085.1:n.3256+67C>T
NM_020983.2:c.3097+67C>T	NP_066193.1:n.3097+67C>T
XM_006719210.2:c.3256+67C>T	XP_006719273.1:n.3256+67C>T
XM_011537810.1:c.2953+67C>T	XP_011536112.1:n.2953+67C>T
XM_011537811.1:c.2794+67C>T	XP_011536113.1:n.2794+67C>T
XR_944483.1:n.3293+67C>T
XM_006719210.4:c.3256+67C>T	XP_006719273.1:n.3256+67C>T
XM_017018743.1:c.2953+67C>T	XP_016874232.1:n.2953+67C>T
XR_001748565.1:n.3714+67C>T
NM_015270.5:c.3256+67C>T MANE Select	NP_056085.1:n.3256+67C>T
NM_001390830.1:c.3097+67C>T	NP_001377759.1:n.3097+67C>T
NM_001390831.1:c.3256+67C>T	NP_001377760.1:n.3256+67C>T