Canonical Allele Identifier: CA354223343

Gene: ADCY5

Linked Data

• dbSNP Id: rs2108193313
• MyVariant Identifiers: chr3:g.123009973G>A (hg19) ; chr3:g.123291126G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291126G>A , CM000665.2:g.123291126G>A	GRCh38
NC_000003.11:g.123009973G>A , CM000665.1:g.123009973G>A	GRCh37
NC_000003.10:g.124492663G>A	NCBI36
NG_033882.1:g.162420C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1991C>T	ENSP00000420082.2:p.Ala664Val
ENST00000470367.2:c.2279C>T	ENSP00000514541.1:p.Ala760Val
ENST00000483566.2:c.1991C>T	ENSP00000420252.2:p.Ala664Val
ENST00000699714.1:c.1991C>T	ENSP00000514539.1:p.Ala664Val
ENST00000699715.1:c.1991C>T	ENSP00000514540.1:p.Ala664Val
ENST00000699716.1:c.1991C>T	ENSP00000514542.1:p.Ala664Val
ENST00000699717.1:n.1717C>T
ENST00000699718.1:c.3389C>T	ENSP00000514543.1:p.Ala1130Val
ENST00000462833.6:c.3314C>T MANE Select	ENSP00000419361.1:p.Ala1105Val
ENST00000309879.9:c.2264C>T	ENSP00000308685.5:p.Ala755Val
ENST00000462833.5:c.3314C>T	ENSP00000419361.1:p.Ala1105Val
ENST00000491190.5:c.2288C>T	ENSP00000418537.1:p.Ala763Val
NM_001199642.1:c.2264C>T	NP_001186571.1:p.Ala755Val
NM_183357.2:c.3314C>T	NP_899200.1:p.Ala1105Val
XM_005247077.2:c.3389C>T	XP_005247134.1:p.Ala1130Val
XM_005247078.1:c.2339C>T	XP_005247135.1:p.Ala780Val
XM_006713483.1:c.2288C>T	XP_006713546.1:p.Ala763Val
XM_006713484.1:c.2066C>T	XP_006713547.1:p.Ala689Val
XM_011512359.1:c.2390C>T	XP_011510661.1:p.Ala797Val
XM_011512360.1:c.2300C>T	XP_011510662.1:p.Ala767Val
XM_011512361.1:c.2066C>T	XP_011510663.1:p.Ala689Val
XM_005247077.4:c.3389C>T	XP_005247134.1:p.Ala1130Val
XM_011512359.2:c.2390C>T	XP_011510661.1:p.Ala797Val
XM_011512360.3:c.2300C>T	XP_011510662.1:p.Ala767Val
XM_017005638.1:c.2291C>T	XP_016861127.1:p.Ala764Val
XM_017005639.1:c.2291C>T	XP_016861128.1:p.Ala764Val
NM_001378259.1:c.3389C>T	NP_001365188.1:p.Ala1130Val
NM_183357.3:c.3314C>T MANE Select	NP_899200.1:p.Ala1105Val