Canonical Allele Identifier: CA2648980683
Community Standard Title: NM_018417.6(ADCY10):c.1140-114A>G
Gene: ADCY10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.167880305T>C , CM000663.2:g.167880305T>C GRCh38
NC_000001.10:g.167849543T>C , CM000663.1:g.167849543T>C GRCh37
NC_000001.9:g.166116167T>C NCBI36
NG_016139.1:g.38911A>G

Transcript Alleles

HGVS Amino-acid Change
NM_018417.6:c.1140-114A>G MANE Select NP_060887.2:n.1140-114A>G
ENST00000367851.9:c.1140-114A>G MANE Select ENSP00000356825.4:n.1140-114A>G
NM_001167749.2:c.681-114A>G NP_001161221.1:n.681-114A>G
NM_001167749.3:c.681-114A>G NP_001161221.1:n.681-114A>G
NM_001297772.1:c.864-114A>G NP_001284701.1:n.864-114A>G
NM_001297772.2:c.864-114A>G NP_001284701.1:n.864-114A>G
NM_018417.5:c.1140-114A>G NP_060887.2:n.1140-114A>G
ENST00000367848.1:c.864-114A>G ENSP00000356822.1:n.864-114A>G
ENST00000367851.8:c.1140-114A>G ENSP00000356825.4:n.1140-114A>G
ENST00000545172.5:c.681-114A>G ENSP00000441992.1:n.681-114A>G
XM_005245330.3:c.1140-114A>G XP_005245387.1:n.1140-114A>G
XM_005245330.5:c.1140-114A>G XP_005245387.1:n.1140-114A>G
XM_006711449.2:c.1140-114A>G XP_006711512.1:n.1140-114A>G
XM_006711449.4:c.1140-114A>G XP_006711512.1:n.1140-114A>G
XM_011509760.1:c.1140-114A>G XP_011508062.1:n.1140-114A>G
XM_011509760.3:c.1140-114A>G XP_011508062.1:n.1140-114A>G
XM_011509761.1:c.1035-114A>G XP_011508063.1:n.1035-114A>G
XM_011509762.1:c.996-114A>G XP_011508064.1:n.996-114A>G
XM_011509762.3:c.996-114A>G XP_011508064.1:n.996-114A>G
XM_011509763.1:c.1140-114A>G XP_011508065.1:n.1140-114A>G
XM_011509763.3:c.1140-114A>G XP_011508065.1:n.1140-114A>G
XM_011509764.1:c.891-114A>G XP_011508066.1:n.891-114A>G
XM_011509765.1:c.864-114A>G XP_011508067.1:n.864-114A>G
XM_011509766.1:c.1140-114A>G XP_011508068.1:n.1140-114A>G
XM_011509766.3:c.1140-114A>G XP_011508068.1:n.1140-114A>G
XM_017001778.2:c.1140-114A>G XP_016857267.1:n.1140-114A>G
XR_921889.1:n.2749-114A>G
XR_921889.3:n.3612-114A>G