Canonical Allele Identifier: CA2697554632

Gene: ADCY10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167896637dup , CM000663.2:g.167896637dup	GRCh38
NC_000001.10:g.167865875dup , CM000663.1:g.167865875dup	GRCh37
NC_000001.9:g.166132499dup	NCBI36
NG_016139.1:g.22579dup

Transcript Alleles

HGVS	Amino-acid Change
NM_018417.6:c.697dup MANE Select	NP_060887.2:p.Cys233LeufsTer12
ENST00000367851.9:c.697dup MANE Select	ENSP00000356825.4:p.Cys233LeufsTer12
NM_001167749.2:c.238dup	NP_001161221.1:p.Cys80LeufsTer12
NM_001167749.3:c.238dup	NP_001161221.1:p.Cys80LeufsTer12
NM_001297772.1:c.421dup	NP_001284701.1:p.Cys141LeufsTer12
NM_001297772.2:c.421dup	NP_001284701.1:p.Cys141LeufsTer12
NM_018417.5:c.697dup	NP_060887.2:p.Cys233LeufsTer12
ENST00000367848.1:c.421dup	ENSP00000356822.1:p.Cys141LeufsTer12
ENST00000367851.8:c.697dup	ENSP00000356825.4:p.Cys233LeufsTer12
ENST00000545172.5:c.238dup	ENSP00000441992.1:p.Cys80LeufsTer12
XM_005245330.3:c.697dup	XP_005245387.1:p.Cys233LeufsTer12
XM_005245330.5:c.697dup	XP_005245387.1:p.Cys233LeufsTer12
XM_006711449.2:c.697dup	XP_006711512.1:p.Cys233LeufsTer12
XM_006711449.4:c.697dup	XP_006711512.1:p.Cys233LeufsTer12
XM_011509760.1:c.697dup	XP_011508062.1:p.Cys233LeufsTer12
XM_011509760.3:c.697dup	XP_011508062.1:p.Cys233LeufsTer12
XM_011509761.1:c.592dup	XP_011508063.1:p.Cys198LeufsTer12
XM_011509762.1:c.553dup	XP_011508064.1:p.Cys185LeufsTer12
XM_011509762.3:c.553dup	XP_011508064.1:p.Cys185LeufsTer12
XM_011509763.1:c.697dup	XP_011508065.1:p.Cys233LeufsTer12
XM_011509763.3:c.697dup	XP_011508065.1:p.Cys233LeufsTer12
XM_011509764.1:c.448dup	XP_011508066.1:p.Cys150LeufsTer12
XM_011509765.1:c.421dup	XP_011508067.1:p.Cys141LeufsTer12
XM_011509766.1:c.697dup	XP_011508068.1:p.Cys233LeufsTer12
XM_011509766.3:c.697dup	XP_011508068.1:p.Cys233LeufsTer12
XM_017001778.2:c.697dup	XP_016857267.1:p.Cys233LeufsTer12
XR_921889.1:n.2306dup
XR_921889.3:n.3169dup