Canonical Allele Identifier: CA2229422988
Gene: ACD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67657780G= , CM000678.2:g.67657780G= GRCh38
NC_000016.9:g.67691683G= , CM000678.1:g.67691683G= GRCh37
NC_000016.8:g.66249184G= NCBI36
NG_042874.1:g.8036C=
NG_054728.1:g.17862G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000602382.6:c.946C= ENSP00000473313.2:p.Leu316=
ENST00000602780.2:n.2285C=
ENST00000602860.6:n.2200C=
ENST00000695641.1:n.2389C=
ENST00000695648.1:c.1262C= ENSP00000512081.1:p.Ala421=
ENST00000695656.1:n.2240C=
ENST00000695657.1:n.1598C=
ENST00000695658.1:c.1103C= ENSP00000512088.1:p.Ala368=
ENST00000695659.1:c.1298C= ENSP00000512089.1:p.Ala433=
ENST00000695662.1:c.*759C= ENSP00000512091.1:n.*759C=
ENST00000695694.1:c.1235C= ENSP00000512105.1:p.Ala412=
ENST00000695695.1:n.1346C=
ENST00000695696.1:n.1327C=
ENST00000695697.1:c.1193C= ENSP00000512106.1:p.Ala398=
ENST00000695698.1:n.1530C=
ENST00000695699.1:n.1700C=
ENST00000695709.1:n.555C=
ENST00000695710.1:n.1914C=
ENST00000695711.1:c.*588C= ENSP00000512109.1:n.*588C=
ENST00000695712.1:c.*1030C= ENSP00000512110.1:n.*1030C=
ENST00000695731.1:c.603C=
ENST00000695732.1:c.719C= ENSP00000512125.1:p.Ala240=
ENST00000695733.1:c.859C= ENSP00000512126.1:p.Leu287=
ENST00000695734.1:c.1280C= ENSP00000512127.1:p.Ala427=
ENST00000219251.13:c.1271C= ENSP00000219251.8:p.Ala424=
ENST00000620761.6:c.1280C= MANE Select ENSP00000478084.1:p.Ala427=
ENST00000219251.12:c.1529C= ENSP00000219251.7:p.Ala510=
ENST00000393919.8:c.1538C= ENSP00000377496.4:p.Ala513=
ENST00000602320.1:c.1232C= ENSP00000473679.2:p.Ala411=
ENST00000602382.5:c.488C=
ENST00000602622.5:n.2279C=
ENST00000602656.1:n.544C=
ENST00000602860.5:n.1718C=
ENST00000620338.4:c.1538C= ENSP00000483117.1:p.Ala513=
ENST00000620761.4:c.1280C= ENSP00000478084.1:p.Ala427=
NM_001082486.1:c.1538C= NP_001075955.1:p.Ala513=
NM_001082487.1:c.1490C= NP_001075956.1:p.Ala497=
NM_022914.2:c.1529C= NP_075065.2:p.Ala510=
XM_005256115.2:c.1451C= XP_005256172.1:p.Ala484=
NM_001082486.2:c.1280C= MANE Select NP_001075955.2:p.Ala427=
NM_022914.3:c.1271C= NP_075065.3:p.Ala424=
XM_005256115.4:c.1451C= XP_005256172.1:p.Ala484=