Canonical Allele Identifier: CA425171963

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046114C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823245C>G , CM000664.2:g.24823245C>G	GRCh38
NC_000002.11:g.25046114C>G , CM000664.1:g.25046114C>G	GRCh37
NC_000002.10:g.24899618C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2850G>C	ENSP00000384484.2:p.Leu950=
ENST00000679454.1:c.2847G>C MANE Select	ENSP00000505261.1:p.Leu949=
ENST00000260600.9:c.2847G>C	ENSP00000260600.5:p.Leu949=
ENST00000405392.5:c.2850G>C	ENSP00000384484.2:p.Leu950=
ENST00000485887.1:n.119G>C
ENST00000606682.5:c.1788G>C	ENSP00000475652.1:p.Leu596=
NM_004036.3:c.2847G>C	NP_004027.2:p.Leu949=
XM_005264104.1:c.2850G>C	XP_005264161.1:p.Leu950=
XM_005264105.1:c.2847G>C	XP_005264162.1:p.Leu949=
XM_006711925.1:c.2916G>C	XP_006711988.1:p.Leu972=
XM_011532489.1:c.2973G>C	XP_011530791.1:p.Leu991=
XM_011532490.1:c.2970G>C	XP_011530792.1:p.Leu990=
XM_011532491.1:c.2907G>C	XP_011530793.1:p.Leu969=
XM_011532492.1:c.2973G>C	XP_011530794.1:p.Leu991=
XM_011532493.1:c.2835G>C	XP_011530795.1:p.Leu945=
XM_011532494.1:c.2775G>C	XP_011530796.1:p.Leu925=
XM_011532495.1:c.2307G>C	XP_011530797.1:p.Leu769=
XM_011532496.1:c.2250G>C	XP_011530798.1:p.Leu750=
NM_001320613.1:c.2850G>C	NP_001307542.1:p.Leu950=
NM_004036.4:c.2847G>C	NP_004027.2:p.Leu949=
XM_011532492.2:c.2973G>C	XP_011530794.1:p.Leu991=
XM_017003186.1:c.2913G>C	XP_016858675.1:p.Leu971=
XM_017003187.1:c.2904G>C	XP_016858676.1:p.Leu968=
XM_017003188.1:c.2970G>C	XP_016858677.1:p.Leu990=
XM_017003189.1:c.2832G>C	XP_016858678.1:p.Leu944=
XM_017003190.1:c.2709G>C	XP_016858679.1:p.Leu903=
XM_017003191.1:c.2337G>C	XP_016858680.1:p.Leu779=
XM_017003192.1:c.2127G>C	XP_016858681.1:p.Leu709=
XM_017003193.1:c.2124G>C	XP_016858682.1:p.Leu708=
NM_001320613.2:c.2850G>C	NP_001307542.1:p.Leu950=
NM_001377128.1:c.2913G>C	NP_001364057.1:p.Leu971=
NM_001377129.1:c.2709G>C	NP_001364058.1:p.Leu903=
NM_001377130.1:c.2332-615G>C	NP_001364059.1:n.2332-615G>C
NM_001377131.1:c.2124G>C	NP_001364060.1:p.Leu708=
NM_001377132.1:c.2847G>C	NP_001364061.1:p.Leu949=
NM_004036.5:c.2847G>C MANE Select	NP_004027.2:p.Leu949=