Canonical Allele Identifier: CA158287015

Gene: ADCY1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45610797T>G , CM000669.2:g.45610797T>G	GRCh38
NC_000007.13:g.45650396T>G , CM000669.1:g.45650396T>G	GRCh37
NC_000007.12:g.45616921T>G	NCBI36
NG_034198.1:g.41658T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021116.4:c.908+300T>G MANE Select	NP_066939.1:n.908+300T>G
ENST00000297323.12:c.908+300T>G MANE Select	ENSP00000297323.7:n.908+300T>G
NM_001281768.1:c.233+300T>G	NP_001268697.1:n.233+300T>G
NM_001281768.2:c.233+300T>G	NP_001268697.1:n.233+300T>G
NM_021116.2:c.908+300T>G	NP_066939.1:n.908+300T>G
NM_021116.3:c.908+300T>G	NP_066939.1:n.908+300T>G
ENST00000297323.11:c.908+300T>G	ENSP00000297323.7:n.908+300T>G
ENST00000432715.5:c.233+300T>G	ENSP00000392721.1:n.233+300T>G
ENST00000621543.1:c.233+300T>G	ENSP00000479770.1:n.233+300T>G
XM_005249584.2:c.908+300T>G	XP_005249641.1:n.908+300T>G
XM_005249584.3:c.908+300T>G	XP_005249641.1:n.908+300T>G
XM_005249585.1:c.908+300T>G	XP_005249642.1:n.908+300T>G
XM_005249585.2:c.908+300T>G	XP_005249642.1:n.908+300T>G