Canonical Allele Identifier: CA392419899

Gene: AP4E1

Linked Data

• dbSNP Id: rs2064890494
• MyVariant Identifiers: chr15:g.51289584A>C (hg19) ; chr15:g.50997387A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50997387A>C , CM000677.2:g.50997387A>C	GRCh38
NC_000015.9:g.51289584A>C , CM000677.1:g.51289584A>C	GRCh37
NC_000015.8:g.49076876A>C	NCBI36
NG_031875.1:g.93716A>C
NG_031875.2:g.93716A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261842.10:c.2408A>C MANE Select	ENSP00000261842.5:p.Lys803Thr
ENST00000261842.9:c.2408A>C	ENSP00000261842.5:p.Lys803Thr
ENST00000558439.5:c.*1532A>C	ENSP00000452712.1:n.*1532A>C
ENST00000560508.1:c.2183A>C	ENSP00000452976.1:p.Lys728Thr
ENST00000561393.5:c.*1452A>C	ENSP00000452711.1:n.*1452A>C
NM_001252127.1:c.2183A>C	NP_001239056.1:p.Lys728Thr
NM_007347.4:c.2408A>C	NP_031373.2:p.Lys803Thr
XM_005254264.2:c.2183A>C	XP_005254321.1:p.Lys728Thr
XM_006720447.2:c.2183A>C	XP_006720510.1:p.Lys728Thr
XM_011521408.1:c.2228A>C	XP_011519710.1:p.Lys743Thr
XM_011521409.1:c.1058A>C	XP_011519711.1:p.Lys353Thr
XM_005254264.4:c.2183A>C	XP_005254321.1:p.Lys728Thr
XM_006720447.4:c.2183A>C	XP_006720510.1:p.Lys728Thr
XM_017022042.2:c.1526A>C	XP_016877531.1:p.Lys509Thr
XR_001751183.1:n.2515A>C
XR_001751184.1:n.2391A>C
NM_007347.5:c.2408A>C MANE Select	NP_031373.2:p.Lys803Thr
NM_001252127.2:c.2183A>C	NP_001239056.1:p.Lys728Thr