Canonical Allele Identifier: CA4137196

Gene: AP5Z1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.4783341C>T , CM000669.2:g.4783341C>T	GRCh38
NC_000007.13:g.4822972C>T , CM000669.1:g.4822972C>T	GRCh37
NC_000007.12:g.4789498C>T	NCBI36
NG_028111.1:g.12711C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014855.3:c.392C>T MANE Select	NP_055670.1:p.Ala131Val
ENST00000649063.2:c.392C>T MANE Select	ENSP00000497815.1:p.Ala131Val
NM_001364858.1:c.-77C>T	NP_001351787.1:n.-77C>T
NM_014855.2:c.392C>T	NP_055670.1:p.Ala131Val
NR_157345.1:n.485C>T
ENST00000348624.4:c.392C>T	ENSP00000297562.4:p.Ala131Val
ENST00000477680.5:n.150C>T
ENST00000477680.6:n.150C>T
ENST00000491375.1:n.19C>T
ENST00000496303.5:n.456C>T
ENST00000496303.6:n.340-348C>T
ENST00000647984.1:c.205C>T	ENSP00000497794.1:p.Pro69Ser
ENST00000648925.1:c.392C>T	ENSP00000496830.1:p.Ala131Val
ENST00000650310.1:c.392C>T	ENSP00000497395.1:p.Ala131Val
ENST00000650451.1:c.180-862C>T	ENSP00000496998.1:n.180-862C>T
XR_242109.1:n.417C>T