Canonical Allele Identifier: CA342730669
Gene: ADAM15 HGNC NCBI
DCST1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155056158C>T , CM000663.2:g.155056158C>T GRCh38
NC_000001.10:g.155028634C>T , CM000663.1:g.155028634C>T GRCh37
NC_000001.9:g.153295258C>T NCBI36
NG_029667.1:g.9873C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356955.7:c.823C>T (ADAM15) MANE Select ENSP00000349436.2:p.Pro275Ser
ENST00000271836.10:c.823C>T (ADAM15) ENSP00000271836.6:p.Pro275Ser
ENST00000355956.6:c.823C>T (ADAM15) ENSP00000348227.2:p.Pro275Ser
ENST00000356955.6:c.823C>T (ADAM15) ENSP00000349436.2:p.Pro275Ser
ENST00000359280.8:c.823C>T (ADAM15) ENSP00000352226.4:p.Pro275Ser
ENST00000360674.8:c.823C>T (ADAM15) ENSP00000353892.4:p.Pro275Ser
ENST00000368412.7:c.823C>T (ADAM15) ENSP00000357397.3:p.Pro275Ser
ENST00000368413.5:c.278-1041C>T (ADAM15) ENSP00000357398.1:n.278-1041C>T
ENST00000447332.3:c.775C>T (ADAM15) ENSP00000476000.1:p.Pro259Ser
ENST00000449910.6:c.823C>T (ADAM15) ENSP00000403843.2:p.Pro275Ser
ENST00000461564.6:n.953C>T (ADAM15)
ENST00000470779.1:n.278C>T (ADAM15)
ENST00000472434.5:n.859C>T (ADAM15)
ENST00000473905.6:n.1101C>T (ADAM15)
ENST00000487956.6:n.821C>T (ADAM15)
ENST00000525020.1:n.63C>T (ADAM15)
ENST00000526491.5:c.823C>T (ADAM15) ENSP00000432347.1:p.Pro275Ser
ENST00000527418.5:n.2469C>T (ADAM15)
ENST00000529473.5:c.823C>T (ADAM15) ENSP00000434227.1:p.Pro275Ser
ENST00000531455.5:c.853C>T (ADAM15) ENSP00000432927.1:p.Pro285Ser
ENST00000534019.1:n.592C>T (ADAM15)
NM_001261464.1:c.853C>T (ADAM15) NP_001248393.1:p.Pro285Ser
NM_001261465.1:c.823C>T (ADAM15) NP_001248394.1:p.Pro275Ser
NM_001261466.1:c.775C>T (ADAM15) NP_001248395.1:p.Pro259Ser
NM_003815.4:c.823C>T (ADAM15) NP_003806.3:p.Pro275Ser
NM_207191.2:c.823C>T (ADAM15) NP_997074.1:p.Pro275Ser
NM_207194.2:c.823C>T (ADAM15) NP_997077.1:p.Pro275Ser
NM_207195.2:c.823C>T (ADAM15) NP_997078.1:p.Pro275Ser
NM_207196.2:c.823C>T (ADAM15) NP_997079.1:p.Pro275Ser
NM_207197.2:c.823C>T (ADAM15) NP_997080.1:p.Pro275Ser
NR_040773.1:n.236-6797G>A (DCST1-AS1)
NR_048577.1:n.938C>T (ADAM15)
NR_048578.1:n.938C>T (ADAM15)
NR_048579.1:n.938C>T (ADAM15)
NM_001261464.2:c.853C>T (ADAM15) NP_001248393.1:p.Pro285Ser
NM_001261465.2:c.823C>T (ADAM15) NP_001248394.1:p.Pro275Ser
NM_001261466.2:c.775C>T (ADAM15) NP_001248395.1:p.Pro259Ser
NM_003815.5:c.823C>T (ADAM15) NP_003806.3:p.Pro275Ser
NM_207191.3:c.823C>T (ADAM15) NP_997074.1:p.Pro275Ser
NM_207194.3:c.823C>T (ADAM15) NP_997077.1:p.Pro275Ser
NM_207195.3:c.823C>T (ADAM15) NP_997078.1:p.Pro275Ser
NM_207196.3:c.823C>T (ADAM15) NP_997079.1:p.Pro275Ser
NM_207197.3:c.823C>T (ADAM15) MANE Select NP_997080.1:p.Pro275Ser
NR_048577.2:n.894C>T (ADAM15)
NR_048578.2:n.894C>T (ADAM15)
NR_048579.2:n.894C>T (ADAM15)