Canonical Allele Identifier: CA2405724600
Gene: ADSL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.40364945T= , CM000684.2:g.40364945T= GRCh38
NC_000022.10:g.40760949T= , CM000684.1:g.40760949T= GRCh37
NC_000022.9:g.39090895T= NCBI36
NG_007993.1:g.23446T=
NG_007993.2:g.23446T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480775.3:c.*651T= ENSP00000485462.2:n.*651T=
ENST00000623287.4:c.*682T= ENSP00000485437.1:n.*682T=
ENST00000623632.4:c.948T= ENSP00000485288.2:p.Gly316=
ENST00000625194.4:c.1299T= ENSP00000485289.2:p.Gly433=
ENST00000636433.1:n.1279T=
ENST00000636714.1:c.1257T= ENSP00000490946.1:p.Gly419=
ENST00000637666.2:c.1191+580T= ENSP00000489696.2:n.1191+580T=
ENST00000637669.1:c.1257T= ENSP00000489728.1:p.Gly419=
ENST00000639722.1:c.*953T= ENSP00000492828.1:n.*953T=
ENST00000674592.1:n.2771T=
ENST00000675622.1:n.4324T=
ENST00000679609.1:c.*867T= ENSP00000506592.1:n.*867T=
ENST00000679656.1:n.1942T=
ENST00000679723.1:c.1212T= ENSP00000505155.1:p.Gly404=
ENST00000679845.1:n.1565T=
ENST00000679904.1:n.1653T=
ENST00000680378.1:c.1344T= ENSP00000505556.1:p.Gly448=
ENST00000680444.1:c.*620T= ENSP00000505298.1:n.*620T=
ENST00000680978.1:c.1257T= ENSP00000505244.1:p.Gly419=
ENST00000681003.1:n.720T=
ENST00000681159.1:n.2661T=
ENST00000216194.11:c.1299T= ENSP00000216194.8:p.Gly433=
ENST00000342312.9:c.1191+580T= ENSP00000341429.6:n.1191+580T=
ENST00000623063.3:c.1257T= MANE Select ENSP00000485525.1:p.Gly419=
ENST00000623387.1:n.388T=
ENST00000625194.3:c.886T=
NM_000026.2:c.1257T= NP_000017.1:p.Gly419=
NM_001123378.1:c.1191+580T= NP_001116850.1:n.1191+580T=
XM_011529976.1:c.1257T= XP_011528278.1:p.Gly419=
XM_011529977.1:c.1257T= XP_011528279.1:p.Gly419=
XM_011529978.1:c.1191+580T= XP_011528280.1:n.1191+580T=
XM_011529979.1:c.1257T= XP_011528281.1:p.Gly419=
XM_011529980.1:c.1191+580T= XP_011528282.1:n.1191+580T=
XM_011529981.1:c.792T= XP_011528283.1:p.Gly264=
XM_011529982.1:c.426T= XP_011528284.1:p.Gly142=
XR_937824.1:n.1347T=
XR_937825.1:n.1281+580T=
NM_000026.3:c.1257T= NP_000017.1:p.Gly419=
NM_001123378.2:c.1191+580T= NP_001116850.1:n.1191+580T=
NM_001317923.1:c.1065T= NP_001304852.1:p.Gly355=
NM_001363840.1:c.1257T= NP_001350769.1:p.Gly419=
NR_134256.1:n.1347T=
XM_011529977.3:c.1257T= XP_011528279.1:p.Gly419=
XM_011529980.3:c.1191+580T= XP_011528282.1:n.1191+580T=
XM_017028636.1:c.1212T= XP_016884125.1:p.Gly404=
XM_017028637.1:c.1212T= XP_016884126.1:p.Gly404=
XM_017028638.1:c.792T= XP_016884127.1:p.Gly264=
XM_017028639.2:c.792T= XP_016884128.1:p.Gly264=
XM_017028640.1:c.426T= XP_016884129.1:p.Gly142=
XM_024452166.1:c.1146+580T= XP_024307934.1:n.1146+580T=
XR_001755176.2:n.1499T=
XR_002958670.1:n.1284T=
XR_937825.3:n.1279+580T=
NM_000026.4:c.1257T= MANE Select NP_000017.1:p.Gly419=
NM_001363840.2:c.1257T= NP_001350769.1:p.Gly419=
NM_001123378.3:c.1191+580T= NP_001116850.1:n.1191+580T=
NM_001317923.2:c.1065T= NP_001304852.1:p.Gly355=
NM_001363840.3:c.1257T= NP_001350769.1:p.Gly419=
NR_134256.2:n.1347T=