Canonical Allele Identifier: CA342727234

Gene: ADAM15 DCST1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155055839C>A , CM000663.2:g.155055839C>A	GRCh38
NC_000001.10:g.155028315C>A , CM000663.1:g.155028315C>A	GRCh37
NC_000001.9:g.153294939C>A	NCBI36
NG_029667.1:g.9554C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356955.7:c.662C>A (ADAM15) MANE Select	ENSP00000349436.2:p.Ala221Asp
ENST00000271836.10:c.662C>A (ADAM15)	ENSP00000271836.6:p.Ala221Asp
ENST00000355956.6:c.662C>A (ADAM15)	ENSP00000348227.2:p.Ala221Asp
ENST00000356955.6:c.662C>A (ADAM15)	ENSP00000349436.2:p.Ala221Asp
ENST00000359280.8:c.662C>A (ADAM15)	ENSP00000352226.4:p.Ala221Asp
ENST00000360674.8:c.662C>A (ADAM15)	ENSP00000353892.4:p.Ala221Asp
ENST00000368412.7:c.662C>A (ADAM15)	ENSP00000357397.3:p.Ala221Asp
ENST00000368413.5:c.278-1360C>A (ADAM15)	ENSP00000357398.1:n.278-1360C>A
ENST00000447332.3:c.614C>A (ADAM15)	ENSP00000476000.1:p.Ala205Asp
ENST00000449910.6:c.662C>A (ADAM15)	ENSP00000403843.2:p.Ala221Asp
ENST00000461564.6:n.792C>A (ADAM15)
ENST00000470779.1:n.38C>A (ADAM15)
ENST00000472434.5:n.698C>A (ADAM15)
ENST00000473905.6:n.940C>A (ADAM15)
ENST00000480331.5:n.867C>A (ADAM15)
ENST00000487956.6:n.674-93C>A (ADAM15)
ENST00000526491.5:c.662C>A (ADAM15)	ENSP00000432347.1:p.Ala221Asp
ENST00000527418.5:n.2308C>A (ADAM15)
ENST00000529473.5:c.662C>A (ADAM15)	ENSP00000434227.1:p.Ala221Asp
ENST00000531455.5:c.692C>A (ADAM15)	ENSP00000432927.1:p.Ala231Asp
ENST00000534019.1:n.431C>A (ADAM15)
NM_001261464.1:c.692C>A (ADAM15)	NP_001248393.1:p.Ala231Asp
NM_001261465.1:c.662C>A (ADAM15)	NP_001248394.1:p.Ala221Asp
NM_001261466.1:c.614C>A (ADAM15)	NP_001248395.1:p.Ala205Asp
NM_003815.4:c.662C>A (ADAM15)	NP_003806.3:p.Ala221Asp
NM_207191.2:c.662C>A (ADAM15)	NP_997074.1:p.Ala221Asp
NM_207194.2:c.662C>A (ADAM15)	NP_997077.1:p.Ala221Asp
NM_207195.2:c.662C>A (ADAM15)	NP_997078.1:p.Ala221Asp
NM_207196.2:c.662C>A (ADAM15)	NP_997079.1:p.Ala221Asp
NM_207197.2:c.662C>A (ADAM15)	NP_997080.1:p.Ala221Asp
NR_040773.1:n.236-6478G>T (DCST1-AS1)
NR_048577.1:n.777C>A (ADAM15)
NR_048578.1:n.777C>A (ADAM15)
NR_048579.1:n.777C>A (ADAM15)
NM_001261464.2:c.692C>A (ADAM15)	NP_001248393.1:p.Ala231Asp
NM_001261465.2:c.662C>A (ADAM15)	NP_001248394.1:p.Ala221Asp
NM_001261466.2:c.614C>A (ADAM15)	NP_001248395.1:p.Ala205Asp
NM_003815.5:c.662C>A (ADAM15)	NP_003806.3:p.Ala221Asp
NM_207191.3:c.662C>A (ADAM15)	NP_997074.1:p.Ala221Asp
NM_207194.3:c.662C>A (ADAM15)	NP_997077.1:p.Ala221Asp
NM_207195.3:c.662C>A (ADAM15)	NP_997078.1:p.Ala221Asp
NM_207196.3:c.662C>A (ADAM15)	NP_997079.1:p.Ala221Asp
NM_207197.3:c.662C>A (ADAM15) MANE Select	NP_997080.1:p.Ala221Asp
NR_048577.2:n.733C>A (ADAM15)
NR_048578.2:n.733C>A (ADAM15)
NR_048579.2:n.733C>A (ADAM15)