Canonical Allele Identifier: CA343096874

Gene: ADCY10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167822139A>C , CM000663.2:g.167822139A>C	GRCh38
NC_000001.10:g.167791377A>C , CM000663.1:g.167791377A>C	GRCh37
NC_000001.9:g.166058001A>C	NCBI36
NG_016139.1:g.97077T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367851.9:c.4171T>G MANE Select	ENSP00000356825.4:p.Phe1391Val
ENST00000367848.1:c.3895T>G	ENSP00000356822.1:p.Phe1299Val
ENST00000367851.8:c.4171T>G	ENSP00000356825.4:p.Phe1391Val
ENST00000485964.5:c.1809T>G
ENST00000545172.5:c.3712T>G	ENSP00000441992.1:p.Phe1238Val
NM_001167749.2:c.3712T>G	NP_001161221.1:p.Phe1238Val
NM_001297772.1:c.3895T>G	NP_001284701.1:p.Phe1299Val
NM_018417.5:c.4171T>G	NP_060887.2:p.Phe1391Val
XM_006711449.2:c.4171T>G	XP_006711512.1:p.Phe1391Val
XM_011509760.1:c.4171T>G	XP_011508062.1:p.Phe1391Val
XM_011509761.1:c.4066T>G	XP_011508063.1:p.Phe1356Val
XM_011509762.1:c.4027T>G	XP_011508064.1:p.Phe1343Val
XM_011509763.1:c.4009T>G	XP_011508065.1:p.Phe1337Val
XM_011509764.1:c.3922T>G	XP_011508066.1:p.Phe1308Val
XM_011509765.1:c.3895T>G	XP_011508067.1:p.Phe1299Val
XR_921889.1:n.5780T>G
XM_006711449.4:c.4171T>G	XP_006711512.1:p.Phe1391Val
XM_011509760.3:c.4171T>G	XP_011508062.1:p.Phe1391Val
XM_011509762.3:c.4027T>G	XP_011508064.1:p.Phe1343Val
XM_011509763.3:c.4009T>G	XP_011508065.1:p.Phe1337Val
XR_921889.3:n.6643T>G
NM_001167749.3:c.3712T>G	NP_001161221.1:p.Phe1238Val
NM_001297772.2:c.3895T>G	NP_001284701.1:p.Phe1299Val
NM_018417.6:c.4171T>G MANE Select	NP_060887.2:p.Phe1391Val