Canonical Allele Identifier: CA346063668

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047332A>G (hg19) ; chr2:g.24824463A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824463A>G , CM000664.2:g.24824463A>G	GRCh38
NC_000002.11:g.25047332A>G , CM000664.1:g.25047332A>G	GRCh37
NC_000002.10:g.24900836A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2654T>C	ENSP00000384484.2:p.Met885Thr
ENST00000679454.1:c.2651T>C MANE Select	ENSP00000505261.1:p.Met884Thr
ENST00000260600.9:c.2651T>C	ENSP00000260600.5:p.Met884Thr
ENST00000405392.5:c.2654T>C	ENSP00000384484.2:p.Met885Thr
ENST00000606682.5:c.1592T>C	ENSP00000475652.1:p.Met531Thr
NM_004036.3:c.2651T>C	NP_004027.2:p.Met884Thr
XM_005264104.1:c.2654T>C	XP_005264161.1:p.Met885Thr
XM_005264105.1:c.2651T>C	XP_005264162.1:p.Met884Thr
XM_006711925.1:c.2720T>C	XP_006711988.1:p.Met907Thr
XM_011532489.1:c.2777T>C	XP_011530791.1:p.Met926Thr
XM_011532490.1:c.2774T>C	XP_011530792.1:p.Met925Thr
XM_011532491.1:c.2711T>C	XP_011530793.1:p.Met904Thr
XM_011532492.1:c.2777T>C	XP_011530794.1:p.Met926Thr
XM_011532493.1:c.2639T>C	XP_011530795.1:p.Met880Thr
XM_011532494.1:c.2579T>C	XP_011530796.1:p.Met860Thr
XM_011532495.1:c.2111T>C	XP_011530797.1:p.Met704Thr
XM_011532496.1:c.2054T>C	XP_011530798.1:p.Met685Thr
NM_001320613.1:c.2654T>C	NP_001307542.1:p.Met885Thr
NM_004036.4:c.2651T>C	NP_004027.2:p.Met884Thr
XM_011532492.2:c.2777T>C	XP_011530794.1:p.Met926Thr
XM_017003186.1:c.2717T>C	XP_016858675.1:p.Met906Thr
XM_017003187.1:c.2708T>C	XP_016858676.1:p.Met903Thr
XM_017003188.1:c.2774T>C	XP_016858677.1:p.Met925Thr
XM_017003189.1:c.2636T>C	XP_016858678.1:p.Met879Thr
XM_017003190.1:c.2513T>C	XP_016858679.1:p.Met838Thr
XM_017003191.1:c.2141T>C	XP_016858680.1:p.Met714Thr
XM_017003192.1:c.1931T>C	XP_016858681.1:p.Met644Thr
XM_017003193.1:c.1928T>C	XP_016858682.1:p.Met643Thr
NM_001320613.2:c.2654T>C	NP_001307542.1:p.Met885Thr
NM_001377128.1:c.2717T>C	NP_001364057.1:p.Met906Thr
NM_001377129.1:c.2513T>C	NP_001364058.1:p.Met838Thr
NM_001377130.1:c.2246T>C	NP_001364059.1:p.Met749Thr
NM_001377131.1:c.1928T>C	NP_001364060.1:p.Met643Thr
NM_001377132.1:c.2651T>C	NP_001364061.1:p.Met884Thr
NM_004036.5:c.2651T>C MANE Select	NP_004027.2:p.Met884Thr