Canonical Allele Identifier: CA392419888

Gene: AP4E1

Linked Data

• MyVariant Identifiers: chr15:g.51289578A>T (hg19) ; chr15:g.50997381A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50997381A>T , CM000677.2:g.50997381A>T	GRCh38
NC_000015.9:g.51289578A>T , CM000677.1:g.51289578A>T	GRCh37
NC_000015.8:g.49076870A>T	NCBI36
NG_031875.1:g.93710A>T
NG_031875.2:g.93710A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261842.10:c.2402A>T MANE Select	ENSP00000261842.5:p.Glu801Val
ENST00000261842.9:c.2402A>T	ENSP00000261842.5:p.Glu801Val
ENST00000558439.5:c.*1526A>T	ENSP00000452712.1:n.*1526A>T
ENST00000560508.1:c.2177A>T	ENSP00000452976.1:p.Glu726Val
ENST00000561393.5:c.*1446A>T	ENSP00000452711.1:n.*1446A>T
NM_001252127.1:c.2177A>T	NP_001239056.1:p.Glu726Val
NM_007347.4:c.2402A>T	NP_031373.2:p.Glu801Val
XM_005254264.2:c.2177A>T	XP_005254321.1:p.Glu726Val
XM_006720447.2:c.2177A>T	XP_006720510.1:p.Glu726Val
XM_011521408.1:c.2222A>T	XP_011519710.1:p.Glu741Val
XM_011521409.1:c.1052A>T	XP_011519711.1:p.Glu351Val
XM_005254264.4:c.2177A>T	XP_005254321.1:p.Glu726Val
XM_006720447.4:c.2177A>T	XP_006720510.1:p.Glu726Val
XM_017022042.2:c.1520A>T	XP_016877531.1:p.Glu507Val
XR_001751183.1:n.2509A>T
XR_001751184.1:n.2385A>T
NM_007347.5:c.2402A>T MANE Select	NP_031373.2:p.Glu801Val
NM_001252127.2:c.2177A>T	NP_001239056.1:p.Glu726Val