Canonical Allele Identifier: CA425172001

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046171G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823302G>C , CM000664.2:g.24823302G>C	GRCh38
NC_000002.11:g.25046171G>C , CM000664.1:g.25046171G>C	GRCh37
NC_000002.10:g.24899675G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2793C>G	ENSP00000384484.2:p.Pro931=
ENST00000679454.1:c.2790C>G MANE Select	ENSP00000505261.1:p.Pro930=
ENST00000260600.9:c.2790C>G	ENSP00000260600.5:p.Pro930=
ENST00000405392.5:c.2793C>G	ENSP00000384484.2:p.Pro931=
ENST00000485887.1:n.62C>G
ENST00000606682.5:c.1731C>G	ENSP00000475652.1:p.Pro577=
NM_004036.3:c.2790C>G	NP_004027.2:p.Pro930=
XM_005264104.1:c.2793C>G	XP_005264161.1:p.Pro931=
XM_005264105.1:c.2790C>G	XP_005264162.1:p.Pro930=
XM_006711925.1:c.2859C>G	XP_006711988.1:p.Pro953=
XM_011532489.1:c.2916C>G	XP_011530791.1:p.Pro972=
XM_011532490.1:c.2913C>G	XP_011530792.1:p.Pro971=
XM_011532491.1:c.2850C>G	XP_011530793.1:p.Pro950=
XM_011532492.1:c.2916C>G	XP_011530794.1:p.Pro972=
XM_011532493.1:c.2778C>G	XP_011530795.1:p.Pro926=
XM_011532494.1:c.2718C>G	XP_011530796.1:p.Pro906=
XM_011532495.1:c.2250C>G	XP_011530797.1:p.Pro750=
XM_011532496.1:c.2193C>G	XP_011530798.1:p.Pro731=
NM_001320613.1:c.2793C>G	NP_001307542.1:p.Pro931=
NM_004036.4:c.2790C>G	NP_004027.2:p.Pro930=
XM_011532492.2:c.2916C>G	XP_011530794.1:p.Pro972=
XM_017003186.1:c.2856C>G	XP_016858675.1:p.Pro952=
XM_017003187.1:c.2847C>G	XP_016858676.1:p.Pro949=
XM_017003188.1:c.2913C>G	XP_016858677.1:p.Pro971=
XM_017003189.1:c.2775C>G	XP_016858678.1:p.Pro925=
XM_017003190.1:c.2652C>G	XP_016858679.1:p.Pro884=
XM_017003191.1:c.2280C>G	XP_016858680.1:p.Pro760=
XM_017003192.1:c.2070C>G	XP_016858681.1:p.Pro690=
XM_017003193.1:c.2067C>G	XP_016858682.1:p.Pro689=
NM_001320613.2:c.2793C>G	NP_001307542.1:p.Pro931=
NM_001377128.1:c.2856C>G	NP_001364057.1:p.Pro952=
NM_001377129.1:c.2652C>G	NP_001364058.1:p.Pro884=
NM_001377130.1:c.2332-672C>G	NP_001364059.1:n.2332-672C>G
NM_001377131.1:c.2067C>G	NP_001364060.1:p.Pro689=
NM_001377132.1:c.2790C>G	NP_001364061.1:p.Pro930=
NM_004036.5:c.2790C>G MANE Select	NP_004027.2:p.Pro930=