Canonical Allele Identifier: CA767114631

Gene: ADCY3

Linked Data

• dbSNP Id: rs5829944
• MyVariant Identifiers: chr2:g.25054107_25054108insAAC (hg19) ; chr2:g.24831238_24831239insAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24831240_24831241insCAA , CM000664.2:g.24831240_24831241insCAA	GRCh38
NC_000002.11:g.25054109_25054110insCAA , CM000664.1:g.25054109_25054110insCAA	GRCh37
NC_000002.10:g.24907613_24907614insCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2056-414_2056-413insGTT	ENSP00000384484.2:n.2056-414_2056-413insGTT
ENST00000679454.1:c.2056-414_2056-413insGTT MANE Select	ENSP00000505261.1:n.2056-414_2056-413insGTT
ENST00000260600.9:c.2056-414_2056-413insGTT	ENSP00000260600.5:n.2056-414_2056-413insGTT
ENST00000405392.5:c.2056-414_2056-413insGTT	ENSP00000384484.2:n.2056-414_2056-413insGTT
ENST00000450524.1:n.149-414_149-413insGTT
ENST00000455323.1:c.73-414_73-413insGTT	ENSP00000402008.1:n.73-414_73-413insGTT
ENST00000606682.5:c.1135-414_1135-413insGTT	ENSP00000475652.1:n.1135-414_1135-413insGTT
NM_004036.3:c.2056-414_2056-413insGTT	NP_004027.2:n.2056-414_2056-413insGTT
XM_005264104.1:c.2056-414_2056-413insGTT	XP_005264161.1:n.2056-414_2056-413insGTT
XM_005264105.1:c.2056-414_2056-413insGTT	XP_005264162.1:n.2056-414_2056-413insGTT
XM_006711925.1:c.2122-414_2122-413insGTT	XP_006711988.1:n.2122-414_2122-413insGTT
XM_011532489.1:c.2179-414_2179-413insGTT	XP_011530791.1:n.2179-414_2179-413insGTT
XM_011532490.1:c.2179-414_2179-413insGTT	XP_011530792.1:n.2179-414_2179-413insGTT
XM_011532491.1:c.2113-414_2113-413insGTT	XP_011530793.1:n.2113-414_2113-413insGTT
XM_011532492.1:c.2179-414_2179-413insGTT	XP_011530794.1:n.2179-414_2179-413insGTT
XM_011532493.1:c.2179-414_2179-413insGTT	XP_011530795.1:n.2179-414_2179-413insGTT
XM_011532494.1:c.2122-414_2122-413insGTT	XP_011530796.1:n.2122-414_2122-413insGTT
XM_011532495.1:c.1513-414_1513-413insGTT	XP_011530797.1:n.1513-414_1513-413insGTT
XM_011532496.1:c.1456-414_1456-413insGTT	XP_011530798.1:n.1456-414_1456-413insGTT
NM_001320613.1:c.2056-414_2056-413insGTT	NP_001307542.1:n.2056-414_2056-413insGTT
NM_004036.4:c.2056-414_2056-413insGTT	NP_004027.2:n.2056-414_2056-413insGTT
XM_011532492.2:c.2179-414_2179-413insGTT	XP_011530794.1:n.2179-414_2179-413insGTT
XM_017003186.1:c.2122-414_2122-413insGTT	XP_016858675.1:n.2122-414_2122-413insGTT
XM_017003187.1:c.2113-414_2113-413insGTT	XP_016858676.1:n.2113-414_2113-413insGTT
XM_017003188.1:c.2179-414_2179-413insGTT	XP_016858677.1:n.2179-414_2179-413insGTT
XM_017003189.1:c.2179-414_2179-413insGTT	XP_016858678.1:n.2179-414_2179-413insGTT
XM_017003190.1:c.2056-414_2056-413insGTT	XP_016858679.1:n.2056-414_2056-413insGTT
XM_017003191.1:c.1543-414_1543-413insGTT	XP_016858680.1:n.1543-414_1543-413insGTT
XM_017003192.1:c.1333-414_1333-413insGTT	XP_016858681.1:n.1333-414_1333-413insGTT
XM_017003193.1:c.1333-414_1333-413insGTT	XP_016858682.1:n.1333-414_1333-413insGTT
NM_001320613.2:c.2056-414_2056-413insGTT	NP_001307542.1:n.2056-414_2056-413insGTT
NM_001377128.1:c.2122-414_2122-413insGTT	NP_001364057.1:n.2122-414_2122-413insGTT
NM_001377129.1:c.2056-414_2056-413insGTT	NP_001364058.1:n.2056-414_2056-413insGTT
NM_001377130.1:c.2056-414_2056-413insGTT	NP_001364059.1:n.2056-414_2056-413insGTT
NM_001377131.1:c.1333-414_1333-413insGTT	NP_001364060.1:n.1333-414_1333-413insGTT
NM_001377132.1:c.2056-414_2056-413insGTT	NP_001364061.1:n.2056-414_2056-413insGTT
NM_004036.5:c.2056-414_2056-413insGTT MANE Select	NP_004027.2:n.2056-414_2056-413insGTT