Canonical Allele Identifier: CA526691434

Gene: ADCY10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167893719dup , CM000663.2:g.167893719dup	GRCh38
NC_000001.10:g.167862957dup , CM000663.1:g.167862957dup	GRCh37
NC_000001.9:g.166129581dup	NCBI36
NG_016139.1:g.25520dup

Transcript Alleles

HGVS	Amino-acid Change
NM_018417.6:c.828+157dup MANE Select	NP_060887.2:n.828+157dup
ENST00000367851.9:c.828+157dup MANE Select	ENSP00000356825.4:n.828+157dup
NM_001167749.2:c.369+157dup	NP_001161221.1:n.369+157dup
NM_001167749.3:c.369+157dup	NP_001161221.1:n.369+157dup
NM_001297772.1:c.552+157dup	NP_001284701.1:n.552+157dup
NM_001297772.2:c.552+157dup	NP_001284701.1:n.552+157dup
NM_018417.5:c.828+157dup	NP_060887.2:n.828+157dup
ENST00000367848.1:c.552+157dup	ENSP00000356822.1:n.552+157dup
ENST00000367851.8:c.828+157dup	ENSP00000356825.4:n.828+157dup
ENST00000545172.5:c.369+157dup	ENSP00000441992.1:n.369+157dup
XM_005245330.3:c.828+157dup	XP_005245387.1:n.828+157dup
XM_005245330.5:c.828+157dup	XP_005245387.1:n.828+157dup
XM_006711449.2:c.828+157dup	XP_006711512.1:n.828+157dup
XM_006711449.4:c.828+157dup	XP_006711512.1:n.828+157dup
XM_011509760.1:c.828+157dup	XP_011508062.1:n.828+157dup
XM_011509760.3:c.828+157dup	XP_011508062.1:n.828+157dup
XM_011509761.1:c.723+157dup	XP_011508063.1:n.723+157dup
XM_011509762.1:c.684+157dup	XP_011508064.1:n.684+157dup
XM_011509762.3:c.684+157dup	XP_011508064.1:n.684+157dup
XM_011509763.1:c.828+157dup	XP_011508065.1:n.828+157dup
XM_011509763.3:c.828+157dup	XP_011508065.1:n.828+157dup
XM_011509764.1:c.579+157dup	XP_011508066.1:n.579+157dup
XM_011509765.1:c.552+157dup	XP_011508067.1:n.552+157dup
XM_011509766.1:c.828+157dup	XP_011508068.1:n.828+157dup
XM_011509766.3:c.828+157dup	XP_011508068.1:n.828+157dup
XM_017001778.2:c.828+157dup	XP_016857267.1:n.828+157dup
XR_921889.1:n.2437+157dup
XR_921889.3:n.3300+157dup