Canonical Allele Identifier: CA4137129

Gene: AP5Z1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.4781659C>T , CM000669.2:g.4781659C>T	GRCh38
NC_000007.13:g.4821290C>T , CM000669.1:g.4821290C>T	GRCh37
NC_000007.12:g.4787816C>T	NCBI36
NG_028111.1:g.11029C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014855.3:c.271C>T MANE Select	NP_055670.1:p.Arg91Ter
ENST00000649063.2:c.271C>T MANE Select	ENSP00000497815.1:p.Arg91Ter
NM_001364858.1:c.-103+347C>T	NP_001351787.1:n.-103+347C>T
NM_014855.2:c.271C>T	NP_055670.1:p.Arg91Ter
NR_157345.1:n.364C>T
ENST00000348624.4:c.271C>T	ENSP00000297562.4:p.Arg91Ter
ENST00000477680.5:n.125-1657C>T
ENST00000477680.6:n.125-1657C>T
ENST00000496303.5:n.335C>T
ENST00000496303.6:n.47C>T
ENST00000647984.1:c.179+347C>T	ENSP00000497794.1:n.179+347C>T
ENST00000648925.1:c.271C>T	ENSP00000496830.1:p.Arg91Ter
ENST00000650310.1:c.271C>T	ENSP00000497395.1:p.Arg91Ter
ENST00000650451.1:c.179+347C>T	ENSP00000496998.1:n.179+347C>T
XR_242109.1:n.296C>T