Canonical Allele Identifier: CA354222544

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123071307A>G (hg19) ; chr3:g.123352460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123352460A>G , CM000665.2:g.123352460A>G	GRCh38
NC_000003.11:g.123071307A>G , CM000665.1:g.123071307A>G	GRCh37
NC_000003.10:g.124553997A>G	NCBI36
NG_033882.1:g.101086T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.-68T>C	ENSP00000420082.2:n.-68T>C
ENST00000470367.2:c.221T>C	ENSP00000514541.1:p.Leu74Pro
ENST00000483566.2:c.-68T>C	ENSP00000420252.2:n.-68T>C
ENST00000699714.1:c.-68T>C	ENSP00000514539.1:n.-68T>C
ENST00000699715.1:c.-68T>C	ENSP00000514540.1:n.-68T>C
ENST00000699716.1:c.-68T>C	ENSP00000514542.1:n.-68T>C
ENST00000699718.1:c.1256T>C	ENSP00000514543.1:p.Leu419Pro
ENST00000462833.6:c.1256T>C MANE Select	ENSP00000419361.1:p.Leu419Pro
ENST00000309879.9:c.206T>C	ENSP00000308685.5:p.Leu69Pro
ENST00000462833.5:c.1256T>C	ENSP00000419361.1:p.Leu419Pro
ENST00000466617.5:c.-68T>C	ENSP00000420082.1:n.-68T>C
ENST00000470367.1:n.551T>C
ENST00000476455.1:c.160T>C	ENSP00000417789.1:p.Ser54Pro
ENST00000483566.1:c.-68T>C	ENSP00000420252.1:n.-68T>C
ENST00000491190.5:c.155T>C	ENSP00000418537.1:p.Leu52Pro
NM_001199642.1:c.206T>C	NP_001186571.1:p.Leu69Pro
NM_183357.2:c.1256T>C	NP_899200.1:p.Leu419Pro
XM_005247077.2:c.1256T>C	XP_005247134.1:p.Leu419Pro
XM_005247078.1:c.206T>C	XP_005247135.1:p.Leu69Pro
XM_006713483.1:c.155T>C	XP_006713546.1:p.Leu52Pro
XM_006713484.1:c.-68T>C	XP_006713547.1:n.-68T>C
XM_011512358.1:c.1256T>C	XP_011510660.1:p.Leu419Pro
XM_011512359.1:c.257T>C	XP_011510661.1:p.Leu86Pro
XM_011512360.1:c.167T>C	XP_011510662.1:p.Leu56Pro
XM_011512361.1:c.-68T>C	XP_011510663.1:n.-68T>C
XM_005247077.4:c.1256T>C	XP_005247134.1:p.Leu419Pro
XM_011512359.2:c.257T>C	XP_011510661.1:p.Leu86Pro
XM_011512360.3:c.167T>C	XP_011510662.1:p.Leu56Pro
XM_017005638.1:c.158T>C	XP_016861127.1:p.Leu53Pro
XM_017005639.1:c.158T>C	XP_016861128.1:p.Leu53Pro
NM_001378259.1:c.1256T>C	NP_001365188.1:p.Leu419Pro
NM_183357.3:c.1256T>C MANE Select	NP_899200.1:p.Leu419Pro