Canonical Allele Identifier: CA354221794

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003477T>A (hg19) ; chr3:g.123284630T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284630T>A , CM000665.2:g.123284630T>A	GRCh38
NC_000003.11:g.123003477T>A , CM000665.1:g.123003477T>A	GRCh37
NC_000003.10:g.124486167T>A	NCBI36
NG_033882.1:g.168916A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2441A>T	ENSP00000420082.2:p.Asn814Ile
ENST00000470367.2:c.2729A>T	ENSP00000514541.1:p.Asn910Ile
ENST00000483566.2:c.2441A>T	ENSP00000420252.2:p.Asn814Ile
ENST00000699714.1:c.2441A>T	ENSP00000514539.1:p.Asn814Ile
ENST00000699715.1:c.2441A>T	ENSP00000514540.1:p.Asn814Ile
ENST00000699716.1:c.2441A>T	ENSP00000514542.1:p.Asn814Ile
ENST00000699717.1:n.2167A>T
ENST00000699718.1:c.3839A>T	ENSP00000514543.1:p.Asn1280Ile
ENST00000462833.6:c.3764A>T MANE Select	ENSP00000419361.1:p.Asn1255Ile
ENST00000309879.9:c.2714A>T	ENSP00000308685.5:p.Asn905Ile
ENST00000462833.5:c.3764A>T	ENSP00000419361.1:p.Asn1255Ile
ENST00000478092.1:n.534A>T
ENST00000491190.5:c.2738A>T	ENSP00000418537.1:p.Asn913Ile
NM_001199642.1:c.2714A>T	NP_001186571.1:p.Asn905Ile
NM_183357.2:c.3764A>T	NP_899200.1:p.Asn1255Ile
XM_005247077.2:c.3839A>T	XP_005247134.1:p.Asn1280Ile
XM_005247078.1:c.2789A>T	XP_005247135.1:p.Asn930Ile
XM_006713483.1:c.2738A>T	XP_006713546.1:p.Asn913Ile
XM_006713484.1:c.2516A>T	XP_006713547.1:p.Asn839Ile
XM_011512359.1:c.2840A>T	XP_011510661.1:p.Asn947Ile
XM_011512360.1:c.2750A>T	XP_011510662.1:p.Asn917Ile
XM_011512361.1:c.2516A>T	XP_011510663.1:p.Asn839Ile
XM_005247077.4:c.3839A>T	XP_005247134.1:p.Asn1280Ile
XM_011512359.2:c.2840A>T	XP_011510661.1:p.Asn947Ile
XM_011512360.3:c.2750A>T	XP_011510662.1:p.Asn917Ile
XM_017005638.1:c.2741A>T	XP_016861127.1:p.Asn914Ile
XM_017005639.1:c.2741A>T	XP_016861128.1:p.Asn914Ile
NM_001378259.1:c.3839A>T	NP_001365188.1:p.Asn1280Ile
NM_183357.3:c.3764A>T MANE Select	NP_899200.1:p.Asn1255Ile