Canonical Allele Identifier: CA2405724623
Gene: ADSL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.40364994A= , CM000684.2:g.40364994A= GRCh38
NC_000022.10:g.40760998A= , CM000684.1:g.40760998A= GRCh37
NC_000022.9:g.39090944A= NCBI36
NG_007993.1:g.23495A=
NG_007993.2:g.23495A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480775.3:c.*700A= ENSP00000485462.2:n.*700A=
ENST00000623287.4:c.*731A= ENSP00000485437.1:n.*731A=
ENST00000623632.4:c.997A= ENSP00000485288.2:p.Ile333=
ENST00000625194.4:c.1348A= ENSP00000485289.2:p.Ile450=
ENST00000636433.1:n.1328A=
ENST00000636714.1:c.1306A= ENSP00000490946.1:p.Ile436=
ENST00000637666.2:c.1191+629A= ENSP00000489696.2:n.1191+629A=
ENST00000637669.1:c.1306A= ENSP00000489728.1:p.Ile436=
ENST00000639722.1:c.*1002A= ENSP00000492828.1:n.*1002A=
ENST00000674592.1:n.2820A=
ENST00000675622.1:n.4373A=
ENST00000679609.1:c.*916A= ENSP00000506592.1:n.*916A=
ENST00000679656.1:n.1991A=
ENST00000679723.1:c.1261A= ENSP00000505155.1:p.Ile421=
ENST00000679845.1:n.1614A=
ENST00000679904.1:n.1702A=
ENST00000680378.1:c.1393A= ENSP00000505556.1:p.Ile465=
ENST00000680444.1:c.*669A= ENSP00000505298.1:n.*669A=
ENST00000680978.1:c.1306A= ENSP00000505244.1:p.Ile436=
ENST00000681003.1:n.769A=
ENST00000681159.1:n.2710A=
ENST00000216194.11:c.1348A= ENSP00000216194.8:p.Ile450=
ENST00000342312.9:c.1191+629A= ENSP00000341429.6:n.1191+629A=
ENST00000423176.6:c.33A=
ENST00000623063.3:c.1306A= MANE Select ENSP00000485525.1:p.Ile436=
ENST00000623387.1:n.437A=
ENST00000623869.3:c.37A= ENSP00000485211.1:p.Ile13=
ENST00000624027.1:c.33A=
ENST00000625194.3:c.935A=
NM_000026.2:c.1306A= NP_000017.1:p.Ile436=
NM_001123378.1:c.1191+629A= NP_001116850.1:n.1191+629A=
XM_011529976.1:c.1306A= XP_011528278.1:p.Ile436=
XM_011529977.1:c.1306A= XP_011528279.1:p.Ile436=
XM_011529978.1:c.1191+629A= XP_011528280.1:n.1191+629A=
XM_011529979.1:c.1306A= XP_011528281.1:p.Ile436=
XM_011529980.1:c.1191+629A= XP_011528282.1:n.1191+629A=
XM_011529981.1:c.841A= XP_011528283.1:p.Ile281=
XM_011529982.1:c.475A= XP_011528284.1:p.Ile159=
XR_937824.1:n.1396A=
XR_937825.1:n.1281+629A=
NM_000026.3:c.1306A= NP_000017.1:p.Ile436=
NM_001123378.2:c.1191+629A= NP_001116850.1:n.1191+629A=
NM_001317923.1:c.1114A= NP_001304852.1:p.Ile372=
NM_001363840.1:c.1306A= NP_001350769.1:p.Ile436=
NR_134256.1:n.1396A=
XM_011529977.3:c.1306A= XP_011528279.1:p.Ile436=
XM_011529980.3:c.1191+629A= XP_011528282.1:n.1191+629A=
XM_017028636.1:c.1261A= XP_016884125.1:p.Ile421=
XM_017028637.1:c.1261A= XP_016884126.1:p.Ile421=
XM_017028638.1:c.841A= XP_016884127.1:p.Ile281=
XM_017028639.2:c.841A= XP_016884128.1:p.Ile281=
XM_017028640.1:c.475A= XP_016884129.1:p.Ile159=
XM_024452166.1:c.1146+629A= XP_024307934.1:n.1146+629A=
XR_001755176.2:n.1548A=
XR_002958670.1:n.1333A=
XR_937825.3:n.1279+629A=
NM_000026.4:c.1306A= MANE Select NP_000017.1:p.Ile436=
NM_001363840.2:c.1306A= NP_001350769.1:p.Ile436=
NM_001123378.3:c.1191+629A= NP_001116850.1:n.1191+629A=
NM_001317923.2:c.1114A= NP_001304852.1:p.Ile372=
NM_001363840.3:c.1306A= NP_001350769.1:p.Ile436=
NR_134256.2:n.1396A=