Canonical Allele Identifier: CA1239072933

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824462C= , CM000664.2:g.24824462C=	GRCh38
NC_000002.11:g.25047331C= , CM000664.1:g.25047331C=	GRCh37
NC_000002.10:g.24900835C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2655G=	ENSP00000384484.2:p.Met885=
ENST00000679454.1:c.2652G= MANE Select	ENSP00000505261.1:p.Met884=
ENST00000260600.9:c.2652G=	ENSP00000260600.5:p.Met884=
ENST00000405392.5:c.2655G=	ENSP00000384484.2:p.Met885=
ENST00000606682.5:c.1593G=	ENSP00000475652.1:p.Met531=
NM_004036.3:c.2652G=	NP_004027.2:p.Met884=
XM_005264104.1:c.2655G=	XP_005264161.1:p.Met885=
XM_005264105.1:c.2652G=	XP_005264162.1:p.Met884=
XM_006711925.1:c.2721G=	XP_006711988.1:p.Met907=
XM_011532489.1:c.2778G=	XP_011530791.1:p.Met926=
XM_011532490.1:c.2775G=	XP_011530792.1:p.Met925=
XM_011532491.1:c.2712G=	XP_011530793.1:p.Met904=
XM_011532492.1:c.2778G=	XP_011530794.1:p.Met926=
XM_011532493.1:c.2640G=	XP_011530795.1:p.Met880=
XM_011532494.1:c.2580G=	XP_011530796.1:p.Met860=
XM_011532495.1:c.2112G=	XP_011530797.1:p.Met704=
XM_011532496.1:c.2055G=	XP_011530798.1:p.Met685=
NM_001320613.1:c.2655G=	NP_001307542.1:p.Met885=
NM_004036.4:c.2652G=	NP_004027.2:p.Met884=
XM_011532492.2:c.2778G=	XP_011530794.1:p.Met926=
XM_017003186.1:c.2718G=	XP_016858675.1:p.Met906=
XM_017003187.1:c.2709G=	XP_016858676.1:p.Met903=
XM_017003188.1:c.2775G=	XP_016858677.1:p.Met925=
XM_017003189.1:c.2637G=	XP_016858678.1:p.Met879=
XM_017003190.1:c.2514G=	XP_016858679.1:p.Met838=
XM_017003191.1:c.2142G=	XP_016858680.1:p.Met714=
XM_017003192.1:c.1932G=	XP_016858681.1:p.Met644=
XM_017003193.1:c.1929G=	XP_016858682.1:p.Met643=
NM_001320613.2:c.2655G=	NP_001307542.1:p.Met885=
NM_001377128.1:c.2718G=	NP_001364057.1:p.Met906=
NM_001377129.1:c.2514G=	NP_001364058.1:p.Met838=
NM_001377130.1:c.2247G=	NP_001364059.1:p.Met749=
NM_001377131.1:c.1929G=	NP_001364060.1:p.Met643=
NM_001377132.1:c.2652G=	NP_001364061.1:p.Met884=
NM_004036.5:c.2652G= MANE Select	NP_004027.2:p.Met884=