Canonical Allele Identifier: CA354221784

Gene: ADCY5

Linked Data

• dbSNP Id: rs1553715736
• MyVariant Identifiers: chr3:g.123003475C>A (hg19) ; chr3:g.123284628C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284628C>A , CM000665.2:g.123284628C>A	GRCh38
NC_000003.11:g.123003475C>A , CM000665.1:g.123003475C>A	GRCh37
NC_000003.10:g.124486165C>A	NCBI36
NG_033882.1:g.168918G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2443G>T	ENSP00000420082.2:p.Gly815Ter
ENST00000470367.2:c.2731G>T	ENSP00000514541.1:p.Gly911Ter
ENST00000483566.2:c.2443G>T	ENSP00000420252.2:p.Gly815Ter
ENST00000699714.1:c.2443G>T	ENSP00000514539.1:p.Gly815Ter
ENST00000699715.1:c.2443G>T	ENSP00000514540.1:p.Gly815Ter
ENST00000699716.1:c.2443G>T	ENSP00000514542.1:p.Gly815Ter
ENST00000699717.1:n.2169G>T
ENST00000699718.1:c.3841G>T	ENSP00000514543.1:p.Gly1281Ter
ENST00000462833.6:c.3766G>T MANE Select	ENSP00000419361.1:p.Gly1256Ter
ENST00000309879.9:c.2716G>T	ENSP00000308685.5:p.Gly906Ter
ENST00000462833.5:c.3766G>T	ENSP00000419361.1:p.Gly1256Ter
ENST00000478092.1:n.536G>T
ENST00000491190.5:c.2740G>T	ENSP00000418537.1:p.Gly914Ter
NM_001199642.1:c.2716G>T	NP_001186571.1:p.Gly906Ter
NM_183357.2:c.3766G>T	NP_899200.1:p.Gly1256Ter
XM_005247077.2:c.3841G>T	XP_005247134.1:p.Gly1281Ter
XM_005247078.1:c.2791G>T	XP_005247135.1:p.Gly931Ter
XM_006713483.1:c.2740G>T	XP_006713546.1:p.Gly914Ter
XM_006713484.1:c.2518G>T	XP_006713547.1:p.Gly840Ter
XM_011512359.1:c.2842G>T	XP_011510661.1:p.Gly948Ter
XM_011512360.1:c.2752G>T	XP_011510662.1:p.Gly918Ter
XM_011512361.1:c.2518G>T	XP_011510663.1:p.Gly840Ter
XM_005247077.4:c.3841G>T	XP_005247134.1:p.Gly1281Ter
XM_011512359.2:c.2842G>T	XP_011510661.1:p.Gly948Ter
XM_011512360.3:c.2752G>T	XP_011510662.1:p.Gly918Ter
XM_017005638.1:c.2743G>T	XP_016861127.1:p.Gly915Ter
XM_017005639.1:c.2743G>T	XP_016861128.1:p.Gly915Ter
NM_001378259.1:c.3841G>T	NP_001365188.1:p.Gly1281Ter
NM_183357.3:c.3766G>T MANE Select	NP_899200.1:p.Gly1256Ter