Canonical Allele Identifier: CA9871584

Linked Data

ClinVar Variation Id: 841399
ClinVar RCV Id: RCV001043610
dbSNP Id: rs750364735

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44623067C>A , CM000682.2:g.44623067C>A GRCh38
NC_000020.10:g.43251708C>A , CM000682.1:g.43251708C>A GRCh37
NC_000020.9:g.42685122C>A NCBI36
NG_007385.1:g.33669G>T , LRG_16:g.33669G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000492931.6:n.709G>T (ADA)
ENST00000536076.2:c.465G>T (ADA) ENSP00000512234.1:p.Lys155Asn
ENST00000536532.6:c.618G>T (ADA) ENSP00000440946.1:p.Lys206Asn
ENST00000537820.2:c.607-137G>T (ADA) ENSP00000441818.1:n.607-137G>T
ENST00000539235.6:c.*2G>T (ADA) ENSP00000446464.1:n.*2G>T
ENST00000695889.1:c.219-137G>T (ADA) ENSP00000512240.1:n.219-137G>T
ENST00000695890.1:n.2421G>T (ADA)
ENST00000695891.1:c.219-137G>T (ADA) ENSP00000512241.1:n.219-137G>T
ENST00000695927.1:c.696G>T (ADA) ENSP00000512270.1:p.Lys232Asn
ENST00000695949.1:c.604-137G>T (ADA) ENSP00000512281.1:n.604-137G>T
ENST00000695957.1:c.*109G>T (ADA) ENSP00000512286.1:n.*109G>T
ENST00000695991.1:c.217-137G>T (ADA) ENSP00000512314.1:n.217-137G>T
ENST00000695992.1:c.618G>T (ADA) ENSP00000512315.1:p.Lys206Asn
ENST00000695993.1:c.618G>T (ADA) ENSP00000512316.1:p.Lys206Asn
ENST00000695994.1:c.618G>T (ADA) ENSP00000512317.1:p.Lys206Asn
ENST00000695995.1:c.228G>T (ADA) ENSP00000512318.1:p.Lys76Asn
ENST00000695996.1:n.689G>T (ADA)
ENST00000696003.1:n.710G>T (ADA)
ENST00000696004.1:n.710G>T (ADA)
ENST00000696005.1:c.129-137G>T (ADA)
ENST00000696006.1:c.607-137G>T (ADA) ENSP00000512325.1:n.607-137G>T
ENST00000696007.1:c.469G>T (ADA) ENSP00000512326.1:n.469G>T
ENST00000696008.1:n.2896G>T (ADA)
ENST00000696017.1:c.615G>T (ADA) ENSP00000512333.1:p.Lys205Asn
ENST00000696034.1:c.618G>T (ADA) ENSP00000512343.1:p.Lys206Asn
ENST00000696035.1:n.728G>T (ADA)
ENST00000696036.1:n.1308G>T (ADA)
ENST00000696037.1:n.2295G>T (ADA)
ENST00000696038.1:c.*364G>T (ADA) ENSP00000512344.1:n.*364G>T
ENST00000696039.1:n.906G>T (ADA)
ENST00000696058.1:c.615G>T (ADA) ENSP00000512361.1:p.Lys205Asn
ENST00000696059.1:c.*563G>T (ADA) ENSP00000512362.1:n.*563G>T
ENST00000696060.1:c.687G>T (ADA) ENSP00000512363.1:p.Lys229Asn
ENST00000696061.1:c.615G>T (ADA) ENSP00000512364.1:p.Lys205Asn
ENST00000696062.1:c.681G>T (ADA) ENSP00000512365.1:p.Lys227Asn
ENST00000696063.1:c.693G>T (ADA) ENSP00000512366.1:p.Lys231Asn
ENST00000696064.1:c.465G>T (ADA) ENSP00000512367.1:p.Lys155Asn
ENST00000696065.1:c.66-137G>T (ADA) ENSP00000512368.1:n.66-137G>T
ENST00000696073.1:n.853G>T (ADA)
ENST00000696074.1:n.234G>T (ADA)
ENST00000696075.1:c.*588G>T (ADA) ENSP00000512374.1:n.*588G>T
ENST00000696076.1:c.687G>T (ADA) ENSP00000512375.1:p.Lys229Asn
ENST00000696077.1:c.612G>T (ADA) ENSP00000512376.1:p.Lys204Asn
ENST00000696078.1:c.615G>T (ADA) ENSP00000512377.1:p.Lys205Asn
ENST00000696079.1:c.615G>T (ADA) ENSP00000512378.1:p.Lys205Asn
ENST00000696080.1:c.618G>T (ADA) ENSP00000512379.1:p.Lys206Asn
ENST00000696081.1:n.737G>T (ADA)
ENST00000696082.1:c.693G>T (ADA) ENSP00000512380.1:p.Lys231Asn
ENST00000696083.1:n.1499G>T (ADA)
ENST00000696084.1:n.719G>T (ADA)
ENST00000696104.1:c.363-137G>T (ADA) ENSP00000512399.1:n.363-137G>T
ENST00000696105.1:c.*159G>T (ADA) ENSP00000512400.1:n.*159G>T
ENST00000372874.9:c.618G>T (ADA) MANE Select ENSP00000361965.4:p.Lys206Asn
ENST00000372874.8:c.618G>T (ADA) ENSP00000361965.4:p.Lys206Asn
ENST00000372887.5:c.152-866C>A (PKIG) ENSP00000361978.1:n.152-866C>A
ENST00000464097.5:n.292G>T (ADA)
ENST00000492931.5:n.702G>T (ADA)
ENST00000536532.5:c.618G>T (ADA) ENSP00000440946.1:p.Lys206Asn
ENST00000537820.1:c.607-137G>T (ADA) ENSP00000441818.1:n.607-137G>T
ENST00000539235.5:c.*2G>T (ADA) ENSP00000446464.1:n.*2G>T
NM_000022.2:c.618G>T , LRG_16t1:c.618G>T (ADA) NP_000013.2:p.Lys206Asn
XM_005260236.2:c.607-137G>T (ADA) XP_005260293.1:n.607-137G>T
XM_011528478.1:c.213G>T (ADA) XP_011526780.1:p.Lys71Asn
XM_011528479.1:c.213G>T (ADA) XP_011526781.1:p.Lys71Asn
XR_244129.1:n.672G>T (ADA)
NM_000022.3:c.618G>T (ADA) NP_000013.2:p.Lys206Asn
NM_001322050.1:c.213G>T (ADA) NP_001308979.1:p.Lys71Asn
NM_001322051.1:c.607-137G>T (ADA) NP_001308980.1:n.607-137G>T
NR_136160.1:n.769G>T (ADA)
NM_000022.4:c.618G>T (ADA) MANE Select NP_000013.2:p.Lys206Asn
NM_001322050.2:c.213G>T (ADA) NP_001308979.1:p.Lys71Asn
NM_001322051.2:c.607-137G>T (ADA) NP_001308980.1:n.607-137G>T
NR_136160.2:n.710G>T (ADA)