Canonical Allele Identifier: CA346063556

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047297A>T (hg19) ; chr2:g.24824428A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824428A>T , CM000664.2:g.24824428A>T	GRCh38
NC_000002.11:g.25047297A>T , CM000664.1:g.25047297A>T	GRCh37
NC_000002.10:g.24900801A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2689T>A	ENSP00000384484.2:p.Leu897Met
ENST00000679454.1:c.2686T>A MANE Select	ENSP00000505261.1:p.Leu896Met
ENST00000260600.9:c.2686T>A	ENSP00000260600.5:p.Leu896Met
ENST00000405392.5:c.2689T>A	ENSP00000384484.2:p.Leu897Met
ENST00000606682.5:c.1627T>A	ENSP00000475652.1:p.Leu543Met
NM_004036.3:c.2686T>A	NP_004027.2:p.Leu896Met
XM_005264104.1:c.2689T>A	XP_005264161.1:p.Leu897Met
XM_005264105.1:c.2686T>A	XP_005264162.1:p.Leu896Met
XM_006711925.1:c.2755T>A	XP_006711988.1:p.Leu919Met
XM_011532489.1:c.2812T>A	XP_011530791.1:p.Leu938Met
XM_011532490.1:c.2809T>A	XP_011530792.1:p.Leu937Met
XM_011532491.1:c.2746T>A	XP_011530793.1:p.Leu916Met
XM_011532492.1:c.2812T>A	XP_011530794.1:p.Leu938Met
XM_011532493.1:c.2674T>A	XP_011530795.1:p.Leu892Met
XM_011532494.1:c.2614T>A	XP_011530796.1:p.Leu872Met
XM_011532495.1:c.2146T>A	XP_011530797.1:p.Leu716Met
XM_011532496.1:c.2089T>A	XP_011530798.1:p.Leu697Met
NM_001320613.1:c.2689T>A	NP_001307542.1:p.Leu897Met
NM_004036.4:c.2686T>A	NP_004027.2:p.Leu896Met
XM_011532492.2:c.2812T>A	XP_011530794.1:p.Leu938Met
XM_017003186.1:c.2752T>A	XP_016858675.1:p.Leu918Met
XM_017003187.1:c.2743T>A	XP_016858676.1:p.Leu915Met
XM_017003188.1:c.2809T>A	XP_016858677.1:p.Leu937Met
XM_017003189.1:c.2671T>A	XP_016858678.1:p.Leu891Met
XM_017003190.1:c.2548T>A	XP_016858679.1:p.Leu850Met
XM_017003191.1:c.2176T>A	XP_016858680.1:p.Leu726Met
XM_017003192.1:c.1966T>A	XP_016858681.1:p.Leu656Met
XM_017003193.1:c.1963T>A	XP_016858682.1:p.Leu655Met
NM_001320613.2:c.2689T>A	NP_001307542.1:p.Leu897Met
NM_001377128.1:c.2752T>A	NP_001364057.1:p.Leu918Met
NM_001377129.1:c.2548T>A	NP_001364058.1:p.Leu850Met
NM_001377130.1:c.2281T>A	NP_001364059.1:p.Leu761Met
NM_001377131.1:c.1963T>A	NP_001364060.1:p.Leu655Met
NM_001377132.1:c.2686T>A	NP_001364061.1:p.Leu896Met
NM_004036.5:c.2686T>A MANE Select	NP_004027.2:p.Leu896Met