Canonical Allele Identifier: CA2749194225

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824451_24824456del , CM000664.2:g.24824451_24824456del	GRCh38
NC_000002.11:g.25047320_25047325del , CM000664.1:g.25047320_25047325del	GRCh37
NC_000002.10:g.24900824_24900829del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2662_2667del	ENSP00000384484.2:p.Trp888_Asn889del
ENST00000679454.1:c.2659_2664del MANE Select	ENSP00000505261.1:p.Trp887_Asn888del
ENST00000260600.9:c.2659_2664del	ENSP00000260600.5:p.Trp887_Asn888del
ENST00000405392.5:c.2662_2667del	ENSP00000384484.2:p.Trp888_Asn889del
ENST00000606682.5:c.1600_1605del	ENSP00000475652.1:p.Trp534_Asn535del
NM_004036.3:c.2659_2664del	NP_004027.2:p.Trp887_Asn888del
XM_005264104.1:c.2662_2667del	XP_005264161.1:p.Trp888_Asn889del
XM_005264105.1:c.2659_2664del	XP_005264162.1:p.Trp887_Asn888del
XM_006711925.1:c.2728_2733del	XP_006711988.1:p.Trp910_Asn911del
XM_011532489.1:c.2785_2790del	XP_011530791.1:p.Trp929_Asn930del
XM_011532490.1:c.2782_2787del	XP_011530792.1:p.Trp928_Asn929del
XM_011532491.1:c.2719_2724del	XP_011530793.1:p.Trp907_Asn908del
XM_011532492.1:c.2785_2790del	XP_011530794.1:p.Trp929_Asn930del
XM_011532493.1:c.2647_2652del	XP_011530795.1:p.Trp883_Asn884del
XM_011532494.1:c.2587_2592del	XP_011530796.1:p.Trp863_Asn864del
XM_011532495.1:c.2119_2124del	XP_011530797.1:p.Trp707_Asn708del
XM_011532496.1:c.2062_2067del	XP_011530798.1:p.Trp688_Asn689del
NM_001320613.1:c.2662_2667del	NP_001307542.1:p.Trp888_Asn889del
NM_004036.4:c.2659_2664del	NP_004027.2:p.Trp887_Asn888del
XM_011532492.2:c.2785_2790del	XP_011530794.1:p.Trp929_Asn930del
XM_017003186.1:c.2725_2730del	XP_016858675.1:p.Trp909_Asn910del
XM_017003187.1:c.2716_2721del	XP_016858676.1:p.Trp906_Asn907del
XM_017003188.1:c.2782_2787del	XP_016858677.1:p.Trp928_Asn929del
XM_017003189.1:c.2644_2649del	XP_016858678.1:p.Trp882_Asn883del
XM_017003190.1:c.2521_2526del	XP_016858679.1:p.Trp841_Asn842del
XM_017003191.1:c.2149_2154del	XP_016858680.1:p.Trp717_Asn718del
XM_017003192.1:c.1939_1944del	XP_016858681.1:p.Trp647_Asn648del
XM_017003193.1:c.1936_1941del	XP_016858682.1:p.Trp646_Asn647del
NM_001320613.2:c.2662_2667del	NP_001307542.1:p.Trp888_Asn889del
NM_001377128.1:c.2725_2730del	NP_001364057.1:p.Trp909_Asn910del
NM_001377129.1:c.2521_2526del	NP_001364058.1:p.Trp841_Asn842del
NM_001377130.1:c.2254_2259del	NP_001364059.1:p.Trp752_Asn753del
NM_001377131.1:c.1936_1941del	NP_001364060.1:p.Trp646_Asn647del
NM_001377132.1:c.2659_2664del	NP_001364061.1:p.Trp887_Asn888del
NM_004036.5:c.2659_2664del MANE Select	NP_004027.2:p.Trp887_Asn888del