Canonical Allele Identifier: CA346063647

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047324A>C (hg19) ; chr2:g.24824455A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824455A>C , CM000664.2:g.24824455A>C	GRCh38
NC_000002.11:g.25047324A>C , CM000664.1:g.25047324A>C	GRCh37
NC_000002.10:g.24900828A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2662T>G	ENSP00000384484.2:p.Trp888Gly
ENST00000679454.1:c.2659T>G MANE Select	ENSP00000505261.1:p.Trp887Gly
ENST00000260600.9:c.2659T>G	ENSP00000260600.5:p.Trp887Gly
ENST00000405392.5:c.2662T>G	ENSP00000384484.2:p.Trp888Gly
ENST00000606682.5:c.1600T>G	ENSP00000475652.1:p.Trp534Gly
NM_004036.3:c.2659T>G	NP_004027.2:p.Trp887Gly
XM_005264104.1:c.2662T>G	XP_005264161.1:p.Trp888Gly
XM_005264105.1:c.2659T>G	XP_005264162.1:p.Trp887Gly
XM_006711925.1:c.2728T>G	XP_006711988.1:p.Trp910Gly
XM_011532489.1:c.2785T>G	XP_011530791.1:p.Trp929Gly
XM_011532490.1:c.2782T>G	XP_011530792.1:p.Trp928Gly
XM_011532491.1:c.2719T>G	XP_011530793.1:p.Trp907Gly
XM_011532492.1:c.2785T>G	XP_011530794.1:p.Trp929Gly
XM_011532493.1:c.2647T>G	XP_011530795.1:p.Trp883Gly
XM_011532494.1:c.2587T>G	XP_011530796.1:p.Trp863Gly
XM_011532495.1:c.2119T>G	XP_011530797.1:p.Trp707Gly
XM_011532496.1:c.2062T>G	XP_011530798.1:p.Trp688Gly
NM_001320613.1:c.2662T>G	NP_001307542.1:p.Trp888Gly
NM_004036.4:c.2659T>G	NP_004027.2:p.Trp887Gly
XM_011532492.2:c.2785T>G	XP_011530794.1:p.Trp929Gly
XM_017003186.1:c.2725T>G	XP_016858675.1:p.Trp909Gly
XM_017003187.1:c.2716T>G	XP_016858676.1:p.Trp906Gly
XM_017003188.1:c.2782T>G	XP_016858677.1:p.Trp928Gly
XM_017003189.1:c.2644T>G	XP_016858678.1:p.Trp882Gly
XM_017003190.1:c.2521T>G	XP_016858679.1:p.Trp841Gly
XM_017003191.1:c.2149T>G	XP_016858680.1:p.Trp717Gly
XM_017003192.1:c.1939T>G	XP_016858681.1:p.Trp647Gly
XM_017003193.1:c.1936T>G	XP_016858682.1:p.Trp646Gly
NM_001320613.2:c.2662T>G	NP_001307542.1:p.Trp888Gly
NM_001377128.1:c.2725T>G	NP_001364057.1:p.Trp909Gly
NM_001377129.1:c.2521T>G	NP_001364058.1:p.Trp841Gly
NM_001377130.1:c.2254T>G	NP_001364059.1:p.Trp752Gly
NM_001377131.1:c.1936T>G	NP_001364060.1:p.Trp646Gly
NM_001377132.1:c.2659T>G	NP_001364061.1:p.Trp887Gly
NM_004036.5:c.2659T>G MANE Select	NP_004027.2:p.Trp887Gly