Canonical Allele Identifier: CA2229423019
Gene: ACD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67657838G= , CM000678.2:g.67657838G= GRCh38
NC_000016.9:g.67691741G= , CM000678.1:g.67691741G= GRCh37
NC_000016.8:g.66249242G= NCBI36
NG_042874.1:g.7978C=
NG_054728.1:g.17920G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000602382.6:c.888C= ENSP00000473313.2:p.Gly296=
ENST00000602780.2:n.2227C=
ENST00000602860.6:n.2142C=
ENST00000695641.1:n.2331C=
ENST00000695648.1:c.1204C= ENSP00000512081.1:p.His402=
ENST00000695656.1:n.2182C=
ENST00000695657.1:n.1540C=
ENST00000695658.1:c.1045C= ENSP00000512088.1:p.His349=
ENST00000695659.1:c.1240C= ENSP00000512089.1:p.His414=
ENST00000695662.1:c.*701C= ENSP00000512091.1:n.*701C=
ENST00000695694.1:c.1177C= ENSP00000512105.1:p.His393=
ENST00000695695.1:n.1288C=
ENST00000695696.1:n.1269C=
ENST00000695697.1:c.1135C= ENSP00000512106.1:p.His379=
ENST00000695698.1:n.1472C=
ENST00000695699.1:n.1642C=
ENST00000695709.1:n.497C=
ENST00000695710.1:n.1856C=
ENST00000695711.1:c.*530C= ENSP00000512109.1:n.*530C=
ENST00000695712.1:c.*972C= ENSP00000512110.1:n.*972C=
ENST00000695731.1:c.545C=
ENST00000695732.1:c.661C= ENSP00000512125.1:p.His221=
ENST00000695733.1:c.801C= ENSP00000512126.1:p.Gly267=
ENST00000695734.1:c.1222C= ENSP00000512127.1:p.His408=
ENST00000219251.13:c.1213C= ENSP00000219251.8:p.His405=
ENST00000620761.6:c.1222C= MANE Select ENSP00000478084.1:p.His408=
ENST00000219251.12:c.1471C= ENSP00000219251.7:p.His491=
ENST00000393919.8:c.1480C= ENSP00000377496.4:p.His494=
ENST00000602320.1:c.1198-24C= ENSP00000473679.2:n.1198-24C=
ENST00000602382.5:c.430C=
ENST00000602622.5:n.2221C=
ENST00000602656.1:n.486C=
ENST00000602860.5:n.1660C=
ENST00000620338.4:c.1480C= ENSP00000483117.1:p.His494=
ENST00000620761.4:c.1222C= ENSP00000478084.1:p.His408=
NM_001082486.1:c.1480C= NP_001075955.1:p.His494=
NM_001082487.1:c.1456-24C= NP_001075956.1:n.1456-24C=
NM_022914.2:c.1471C= NP_075065.2:p.His491=
XM_005256115.2:c.1393C= XP_005256172.1:p.His465=
NM_001082486.2:c.1222C= MANE Select NP_001075955.2:p.His408=
NM_022914.3:c.1213C= NP_075065.3:p.His405=
XM_005256115.4:c.1393C= XP_005256172.1:p.His465=