Canonical Allele Identifier: CA4138253

Gene: AP5Z1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.4790723C>T , CM000669.2:g.4790723C>T	GRCh38
NC_000007.13:g.4830354C>T , CM000669.1:g.4830354C>T	GRCh37
NC_000007.12:g.4796880C>T	NCBI36
NG_028111.1:g.20093C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014855.3:c.1989C>T MANE Select	NP_055670.1:p.Thr663=
ENST00000649063.2:c.1989C>T MANE Select	ENSP00000497815.1:p.Thr663=
NM_001364858.1:c.1521C>T	NP_001351787.1:p.Thr507=
NM_014855.2:c.1989C>T	NP_055670.1:p.Thr663=
NR_157345.1:n.2120C>T
ENST00000348624.4:c.1989C>T	ENSP00000297562.4:p.Thr663=
ENST00000469614.1:n.1537C>T
ENST00000477680.5:n.2276C>T
ENST00000477680.6:n.2276C>T
ENST00000490487.1:n.227-87C>T
ENST00000496303.5:n.2298C>T
ENST00000496303.6:n.1817C>T
ENST00000647984.1:c.*1334C>T	ENSP00000497794.1:n.*1334C>T
ENST00000648237.1:c.227-87C>T
ENST00000648360.1:c.669C>T
ENST00000648925.1:c.*392C>T	ENSP00000496830.1:n.*392C>T
ENST00000649315.1:c.1486C>T
ENST00000649419.1:n.1868C>T
ENST00000649736.1:n.852C>T
ENST00000650310.1:c.*560C>T	ENSP00000497395.1:n.*560C>T
ENST00000650581.1:c.608-87C>T