Canonical Allele Identifier: CA2229422947
Gene: ACD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67657701G= , CM000678.2:g.67657701G= GRCh38
NC_000016.9:g.67691604G= , CM000678.1:g.67691604G= GRCh37
NC_000016.8:g.66249105G= NCBI36
NG_042874.1:g.8115C=
NG_054728.1:g.17783G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000602382.6:c.965-17C= ENSP00000473313.2:n.965-17C=
ENST00000602780.2:n.2364C=
ENST00000602860.6:n.2219-17C=
ENST00000695641.1:n.2408-17C=
ENST00000695648.1:c.1281-17C= ENSP00000512081.1:n.1281-17C=
ENST00000695656.1:n.2319C=
ENST00000695657.1:n.1617-17C=
ENST00000695658.1:c.1122-17C= ENSP00000512088.1:n.1122-17C=
ENST00000695659.1:c.1317-17C= ENSP00000512089.1:n.1317-17C=
ENST00000695662.1:c.*778-17C= ENSP00000512091.1:n.*778-17C=
ENST00000695694.1:c.1254-17C= ENSP00000512105.1:n.1254-17C=
ENST00000695695.1:n.1365-17C=
ENST00000695696.1:n.1346-17C=
ENST00000695697.1:c.1212-17C= ENSP00000512106.1:n.1212-17C=
ENST00000695698.1:n.1549-17C=
ENST00000695709.1:n.574-17C=
ENST00000695711.1:c.*607-17C= ENSP00000512109.1:n.*607-17C=
ENST00000695712.1:c.*1049-17C= ENSP00000512110.1:n.*1049-17C=
ENST00000695731.1:c.622-17C=
ENST00000695732.1:c.738-17C= ENSP00000512125.1:n.738-17C=
ENST00000695733.1:c.878-17C= ENSP00000512126.1:n.878-17C=
ENST00000695734.1:c.1299C= ENSP00000512127.1:p.Ser433=
ENST00000219251.13:c.1290-17C= ENSP00000219251.8:n.1290-17C=
ENST00000620761.6:c.1299-17C= MANE Select ENSP00000478084.1:n.1299-17C=
ENST00000219251.12:c.1548-17C= ENSP00000219251.7:n.1548-17C=
ENST00000393919.8:c.1557-17C= ENSP00000377496.4:n.1557-17C=
ENST00000602320.1:c.1251-17C= ENSP00000473679.2:n.1251-17C=
ENST00000602382.5:c.507-17C=
ENST00000602622.5:n.2358C=
ENST00000602656.1:n.563-17C=
ENST00000602860.5:n.1737-17C=
ENST00000620338.4:c.1557-17C= ENSP00000483117.1:n.1557-17C=
ENST00000620761.4:c.1299-17C= ENSP00000478084.1:n.1299-17C=
NM_001082486.1:c.1557-17C= NP_001075955.1:n.1557-17C=
NM_001082487.1:c.1509-17C= NP_001075956.1:n.1509-17C=
NM_022914.2:c.1548-17C= NP_075065.2:n.1548-17C=
XM_005256115.2:c.1470-17C= XP_005256172.1:n.1470-17C=
NM_001082486.2:c.1299-17C= MANE Select NP_001075955.2:n.1299-17C=
NM_022914.3:c.1290-17C= NP_075065.3:n.1290-17C=
XM_005256115.4:c.1470-17C= XP_005256172.1:n.1470-17C=