Canonical Allele Identifier: CA1136629
Gene: ADAM15 HGNC NCBI
DCST1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155051441C>T , CM000663.2:g.155051441C>T GRCh38
NC_000001.10:g.155023917C>T , CM000663.1:g.155023917C>T GRCh37
NC_000001.9:g.153290541C>T NCBI36
NG_027536.1:g.22636C>T
NG_029667.1:g.5156C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356955.7:c.55C>T (ADAM15) MANE Select ENSP00000349436.2:p.Pro19Ser
ENST00000271836.10:c.55C>T (ADAM15) ENSP00000271836.6:p.Pro19Ser
ENST00000355956.6:c.55C>T (ADAM15) ENSP00000348227.2:p.Pro19Ser
ENST00000356955.6:c.55C>T (ADAM15) ENSP00000349436.2:p.Pro19Ser
ENST00000359280.8:c.55C>T (ADAM15) ENSP00000352226.4:p.Pro19Ser
ENST00000360674.8:c.55C>T (ADAM15) ENSP00000353892.4:p.Pro19Ser
ENST00000368412.7:c.55C>T (ADAM15) ENSP00000357397.3:p.Pro19Ser
ENST00000368413.5:c.55C>T (ADAM15) ENSP00000357398.1:p.Pro19Ser
ENST00000447332.3:c.55C>T (ADAM15) ENSP00000476000.1:p.Pro19Ser
ENST00000449910.6:c.55C>T (ADAM15) ENSP00000403843.2:p.Pro19Ser
ENST00000461564.6:n.134C>T (ADAM15)
ENST00000472434.5:n.88C>T (ADAM15)
ENST00000473905.6:n.357+519C>T (ADAM15)
ENST00000477533.5:n.138C>T (ADAM15)
ENST00000480331.5:n.196+519C>T (ADAM15)
ENST00000485346.6:n.126C>T (ADAM15)
ENST00000487956.6:n.116C>T (ADAM15)
ENST00000526491.5:c.55C>T (ADAM15) ENSP00000432347.1:p.Pro19Ser
ENST00000527418.5:n.496C>T (ADAM15)
ENST00000529473.5:c.55C>T (ADAM15) ENSP00000434227.1:p.Pro19Ser
ENST00000531455.5:c.55C>T (ADAM15) ENSP00000432927.1:p.Pro19Ser
ENST00000531703.5:n.139C>T (ADAM15)
ENST00000531831.5:n.91C>T (ADAM15)
ENST00000533732.5:n.226+535C>T (ADAM15)
NM_001261464.1:c.55C>T (ADAM15) NP_001248393.1:p.Pro19Ser
NM_001261465.1:c.55C>T (ADAM15) NP_001248394.1:p.Pro19Ser
NM_001261466.1:c.55C>T (ADAM15) NP_001248395.1:p.Pro19Ser
NM_003815.4:c.55C>T (ADAM15) NP_003806.3:p.Pro19Ser
NM_207191.2:c.55C>T (ADAM15) NP_997074.1:p.Pro19Ser
NM_207194.2:c.55C>T (ADAM15) NP_997077.1:p.Pro19Ser
NM_207195.2:c.55C>T (ADAM15) NP_997078.1:p.Pro19Ser
NM_207196.2:c.55C>T (ADAM15) NP_997079.1:p.Pro19Ser
NM_207197.2:c.55C>T (ADAM15) NP_997080.1:p.Pro19Ser
NR_040773.1:n.236-2080G>A (DCST1-AS1)
NR_048577.1:n.170C>T (ADAM15)
NR_048578.1:n.170C>T (ADAM15)
NR_048579.1:n.170C>T (ADAM15)
NM_001261464.2:c.55C>T (ADAM15) NP_001248393.1:p.Pro19Ser
NM_001261465.2:c.55C>T (ADAM15) NP_001248394.1:p.Pro19Ser
NM_001261466.2:c.55C>T (ADAM15) NP_001248395.1:p.Pro19Ser
NM_003815.5:c.55C>T (ADAM15) NP_003806.3:p.Pro19Ser
NM_207191.3:c.55C>T (ADAM15) NP_997074.1:p.Pro19Ser
NM_207194.3:c.55C>T (ADAM15) NP_997077.1:p.Pro19Ser
NM_207195.3:c.55C>T (ADAM15) NP_997078.1:p.Pro19Ser
NM_207196.3:c.55C>T (ADAM15) NP_997079.1:p.Pro19Ser
NM_207197.3:c.55C>T (ADAM15) MANE Select NP_997080.1:p.Pro19Ser
NR_048577.2:n.126C>T (ADAM15)
NR_048578.2:n.126C>T (ADAM15)
NR_048579.2:n.126C>T (ADAM15)