Canonical Allele Identifier: CA1137272

Gene: ADAM15 DCST1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155059960C>T , CM000663.2:g.155059960C>T	GRCh38
NC_000001.10:g.155032436C>T , CM000663.1:g.155032436C>T	GRCh37
NC_000001.9:g.153299060C>T	NCBI36
NG_029561.1:g.1224C>T
NG_029667.1:g.13675C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356955.7:c.2054C>T (ADAM15) MANE Select	ENSP00000349436.2:p.Thr685Ile
ENST00000271836.10:c.2054C>T (ADAM15)	ENSP00000271836.6:p.Thr685Ile
ENST00000355956.6:c.2054C>T (ADAM15)	ENSP00000348227.2:p.Thr685Ile
ENST00000356955.6:c.2054C>T (ADAM15)	ENSP00000349436.2:p.Thr685Ile
ENST00000359280.8:c.2054C>T (ADAM15)	ENSP00000352226.4:p.Thr685Ile
ENST00000360674.8:c.2054C>T (ADAM15)	ENSP00000353892.4:p.Thr685Ile
ENST00000368412.7:c.2054C>T (ADAM15)	ENSP00000357397.3:p.Thr685Ile
ENST00000368413.5:c.1172C>T (ADAM15)	ENSP00000357398.1:p.Thr391Ile
ENST00000449910.6:c.2054C>T (ADAM15)	ENSP00000403843.2:p.Thr685Ile
ENST00000461234.5:n.333C>T (ADAM15)
ENST00000461564.6:n.2184C>T (ADAM15)
ENST00000462116.5:n.94C>T (ADAM15)
ENST00000472434.5:n.2090C>T (ADAM15)
ENST00000474709.5:n.137C>T (ADAM15)
ENST00000498481.6:n.340C>T (ADAM15)
ENST00000526491.5:c.2054C>T (ADAM15)	ENSP00000432347.1:p.Thr685Ile
ENST00000527418.5:n.3700C>T (ADAM15)
ENST00000529473.5:c.2054C>T (ADAM15)	ENSP00000434227.1:p.Thr685Ile
ENST00000531455.5:c.2084C>T (ADAM15)	ENSP00000432927.1:p.Thr695Ile
NM_001261464.1:c.2084C>T (ADAM15)	NP_001248393.1:p.Thr695Ile
NM_001261465.1:c.2054C>T (ADAM15)	NP_001248394.1:p.Thr685Ile
NM_003815.4:c.2054C>T (ADAM15)	NP_003806.3:p.Thr685Ile
NM_207191.2:c.2054C>T (ADAM15)	NP_997074.1:p.Thr685Ile
NM_207194.2:c.2054C>T (ADAM15)	NP_997077.1:p.Thr685Ile
NM_207195.2:c.2054C>T (ADAM15)	NP_997078.1:p.Thr685Ile
NM_207196.2:c.2054C>T (ADAM15)	NP_997079.1:p.Thr685Ile
NM_207197.2:c.2054C>T (ADAM15)	NP_997080.1:p.Thr685Ile
NR_040773.1:n.235+3797G>A (DCST1-AS1)
NR_048577.1:n.2169C>T (ADAM15)
NR_048578.1:n.2169C>T (ADAM15)
NR_048579.1:n.2169C>T (ADAM15)
NM_001261464.2:c.2084C>T (ADAM15)	NP_001248393.1:p.Thr695Ile
NM_001261465.2:c.2054C>T (ADAM15)	NP_001248394.1:p.Thr685Ile
NM_003815.5:c.2054C>T (ADAM15)	NP_003806.3:p.Thr685Ile
NM_207191.3:c.2054C>T (ADAM15)	NP_997074.1:p.Thr685Ile
NM_207194.3:c.2054C>T (ADAM15)	NP_997077.1:p.Thr685Ile
NM_207195.3:c.2054C>T (ADAM15)	NP_997078.1:p.Thr685Ile
NM_207196.3:c.2054C>T (ADAM15)	NP_997079.1:p.Thr685Ile
NM_207197.3:c.2054C>T (ADAM15) MANE Select	NP_997080.1:p.Thr685Ile
NR_048577.2:n.2125C>T (ADAM15)
NR_048578.2:n.2125C>T (ADAM15)
NR_048579.2:n.2125C>T (ADAM15)