Canonical Allele Identifier: CA4137024
Community Standard Title: NM_014855.3(AP5Z1):c.49C>T (p.Gln17Ter)
Gene: AP5Z1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.4781182C>T , CM000669.2:g.4781182C>T GRCh38
NC_000007.13:g.4820813C>T , CM000669.1:g.4820813C>T GRCh37
NC_000007.12:g.4787339C>T NCBI36
NG_028111.1:g.10552C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014855.3:c.49C>T MANE Select NP_055670.1:p.Gln17Ter
ENST00000649063.2:c.49C>T MANE Select ENSP00000497815.1:p.Gln17Ter
NM_001364858.1:c.-233C>T NP_001351787.1:n.-233C>T
NM_014855.2:c.49C>T NP_055670.1:p.Gln17Ter
NR_157345.1:n.142C>T
ENST00000348624.4:c.49C>T ENSP00000297562.4:p.Gln17Ter
ENST00000477680.5:n.125-2134C>T
ENST00000477680.6:n.125-2134C>T
ENST00000496303.5:n.113C>T
ENST00000647984.1:c.49C>T ENSP00000497794.1:p.Gln17Ter
ENST00000648925.1:c.49C>T ENSP00000496830.1:p.Gln17Ter
ENST00000650310.1:c.49C>T ENSP00000497395.1:p.Gln17Ter
ENST00000650451.1:c.49C>T ENSP00000496998.1:p.Gln17Ter
XR_242109.1:n.74C>T