Canonical Allele Identifier: CA2405724586
Gene: ADSL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.40364912G= , CM000684.2:g.40364912G= GRCh38
NC_000022.10:g.40760916G= , CM000684.1:g.40760916G= GRCh37
NC_000022.9:g.39090862G= NCBI36
NG_007993.1:g.23413G=
NG_007993.2:g.23413G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480775.3:c.*618G= ENSP00000485462.2:n.*618G=
ENST00000623287.4:c.*649G= ENSP00000485437.1:n.*649G=
ENST00000623632.4:c.915G= ENSP00000485288.2:p.Gln305=
ENST00000625194.4:c.1266G= ENSP00000485289.2:p.Gln422=
ENST00000636433.1:n.1246G=
ENST00000636714.1:c.1224G= ENSP00000490946.1:p.Gln408=
ENST00000637666.2:c.1191+547G= ENSP00000489696.2:n.1191+547G=
ENST00000637669.1:c.1224G= ENSP00000489728.1:p.Gln408=
ENST00000639722.1:c.*920G= ENSP00000492828.1:n.*920G=
ENST00000674592.1:n.2738G=
ENST00000675622.1:n.4291G=
ENST00000679609.1:c.*834G= ENSP00000506592.1:n.*834G=
ENST00000679656.1:n.1909G=
ENST00000679723.1:c.1179G= ENSP00000505155.1:p.Gln393=
ENST00000679845.1:n.1532G=
ENST00000679904.1:n.1620G=
ENST00000680378.1:c.1311G= ENSP00000505556.1:p.Gln437=
ENST00000680444.1:c.*587G= ENSP00000505298.1:n.*587G=
ENST00000680978.1:c.1224G= ENSP00000505244.1:p.Gln408=
ENST00000681003.1:n.687G=
ENST00000681159.1:n.2628G=
ENST00000216194.11:c.1266G= ENSP00000216194.8:p.Gln422=
ENST00000342312.9:c.1191+547G= ENSP00000341429.6:n.1191+547G=
ENST00000623063.3:c.1224G= MANE Select ENSP00000485525.1:p.Gln408=
ENST00000623387.1:n.355G=
ENST00000625194.3:c.853G=
NM_000026.2:c.1224G= NP_000017.1:p.Gln408=
NM_001123378.1:c.1191+547G= NP_001116850.1:n.1191+547G=
XM_011529976.1:c.1224G= XP_011528278.1:p.Gln408=
XM_011529977.1:c.1224G= XP_011528279.1:p.Gln408=
XM_011529978.1:c.1191+547G= XP_011528280.1:n.1191+547G=
XM_011529979.1:c.1224G= XP_011528281.1:p.Gln408=
XM_011529980.1:c.1191+547G= XP_011528282.1:n.1191+547G=
XM_011529981.1:c.759G= XP_011528283.1:p.Gln253=
XM_011529982.1:c.393G= XP_011528284.1:p.Gln131=
XR_937824.1:n.1314G=
XR_937825.1:n.1281+547G=
NM_000026.3:c.1224G= NP_000017.1:p.Gln408=
NM_001123378.2:c.1191+547G= NP_001116850.1:n.1191+547G=
NM_001317923.1:c.1032G= NP_001304852.1:p.Gln344=
NM_001363840.1:c.1224G= NP_001350769.1:p.Gln408=
NR_134256.1:n.1314G=
XM_011529977.3:c.1224G= XP_011528279.1:p.Gln408=
XM_011529980.3:c.1191+547G= XP_011528282.1:n.1191+547G=
XM_017028636.1:c.1179G= XP_016884125.1:p.Gln393=
XM_017028637.1:c.1179G= XP_016884126.1:p.Gln393=
XM_017028638.1:c.759G= XP_016884127.1:p.Gln253=
XM_017028639.2:c.759G= XP_016884128.1:p.Gln253=
XM_017028640.1:c.393G= XP_016884129.1:p.Gln131=
XM_024452166.1:c.1146+547G= XP_024307934.1:n.1146+547G=
XR_001755176.2:n.1466G=
XR_002958670.1:n.1251G=
XR_937825.3:n.1279+547G=
NM_000026.4:c.1224G= MANE Select NP_000017.1:p.Gln408=
NM_001363840.2:c.1224G= NP_001350769.1:p.Gln408=
NM_001123378.3:c.1191+547G= NP_001116850.1:n.1191+547G=
NM_001317923.2:c.1032G= NP_001304852.1:p.Gln344=
NM_001363840.3:c.1224G= NP_001350769.1:p.Gln408=
NR_134256.2:n.1314G=