Canonical Allele Identifier: CA1137050

Gene: ADAM15 DCST1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155057318A>G , CM000663.2:g.155057318A>G	GRCh38
NC_000001.10:g.155029794A>G , CM000663.1:g.155029794A>G	GRCh37
NC_000001.9:g.153296418A>G	NCBI36
NG_029667.1:g.11033A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356955.7:c.1279A>G (ADAM15) MANE Select	ENSP00000349436.2:p.Met427Val
ENST00000271836.10:c.1279A>G (ADAM15)	ENSP00000271836.6:p.Met427Val
ENST00000355956.6:c.1279A>G (ADAM15)	ENSP00000348227.2:p.Met427Val
ENST00000356955.6:c.1279A>G (ADAM15)	ENSP00000349436.2:p.Met427Val
ENST00000359280.8:c.1279A>G (ADAM15)	ENSP00000352226.4:p.Met427Val
ENST00000360674.8:c.1279A>G (ADAM15)	ENSP00000353892.4:p.Met427Val
ENST00000368412.7:c.1279A>G (ADAM15)	ENSP00000357397.3:p.Met427Val
ENST00000368413.5:c.397A>G (ADAM15)	ENSP00000357398.1:p.Met133Val
ENST00000447332.3:c.1231A>G (ADAM15)	ENSP00000476000.1:p.Met411Val
ENST00000449910.6:c.1279A>G (ADAM15)	ENSP00000403843.2:p.Met427Val
ENST00000461564.6:n.1409A>G (ADAM15)
ENST00000472434.5:n.1315A>G (ADAM15)
ENST00000526491.5:c.1279A>G (ADAM15)	ENSP00000432347.1:p.Met427Val
ENST00000527418.5:n.2925A>G (ADAM15)
ENST00000529473.5:c.1279A>G (ADAM15)	ENSP00000434227.1:p.Met427Val
ENST00000531455.5:c.1309A>G (ADAM15)	ENSP00000432927.1:p.Met437Val
NM_001261464.1:c.1309A>G (ADAM15)	NP_001248393.1:p.Met437Val
NM_001261465.1:c.1279A>G (ADAM15)	NP_001248394.1:p.Met427Val
NM_001261466.1:c.1231A>G (ADAM15)	NP_001248395.1:p.Met411Val
NM_003815.4:c.1279A>G (ADAM15)	NP_003806.3:p.Met427Val
NM_207191.2:c.1279A>G (ADAM15)	NP_997074.1:p.Met427Val
NM_207194.2:c.1279A>G (ADAM15)	NP_997077.1:p.Met427Val
NM_207195.2:c.1279A>G (ADAM15)	NP_997078.1:p.Met427Val
NM_207196.2:c.1279A>G (ADAM15)	NP_997079.1:p.Met427Val
NM_207197.2:c.1279A>G (ADAM15)	NP_997080.1:p.Met427Val
NR_040773.1:n.235+6439T>C (DCST1-AS1)
NR_048577.1:n.1394A>G (ADAM15)
NR_048578.1:n.1394A>G (ADAM15)
NR_048579.1:n.1394A>G (ADAM15)
NM_001261464.2:c.1309A>G (ADAM15)	NP_001248393.1:p.Met437Val
NM_001261465.2:c.1279A>G (ADAM15)	NP_001248394.1:p.Met427Val
NM_001261466.2:c.1231A>G (ADAM15)	NP_001248395.1:p.Met411Val
NM_003815.5:c.1279A>G (ADAM15)	NP_003806.3:p.Met427Val
NM_207191.3:c.1279A>G (ADAM15)	NP_997074.1:p.Met427Val
NM_207194.3:c.1279A>G (ADAM15)	NP_997077.1:p.Met427Val
NM_207195.3:c.1279A>G (ADAM15)	NP_997078.1:p.Met427Val
NM_207196.3:c.1279A>G (ADAM15)	NP_997079.1:p.Met427Val
NM_207197.3:c.1279A>G (ADAM15) MANE Select	NP_997080.1:p.Met427Val
NR_048577.2:n.1350A>G (ADAM15)
NR_048578.2:n.1350A>G (ADAM15)
NR_048579.2:n.1350A>G (ADAM15)