Canonical Allele Identifier: CA7558872

Gene: AP4E1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50930864A>C , CM000677.2:g.50930864A>C	GRCh38
NC_000015.9:g.51223061A>C , CM000677.1:g.51223061A>C	GRCh37
NC_000015.8:g.49010353A>C	NCBI36
NG_031875.1:g.27193A>C
NG_031875.2:g.27193A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_007347.5:c.762A>C MANE Select	NP_031373.2:p.Val254=
ENST00000261842.10:c.762A>C MANE Select	ENSP00000261842.5:p.Val254=
NM_001252127.1:c.537A>C	NP_001239056.1:p.Val179=
NM_001252127.2:c.537A>C	NP_001239056.1:p.Val179=
NM_007347.4:c.762A>C	NP_031373.2:p.Val254=
ENST00000261842.9:c.762A>C	ENSP00000261842.5:p.Val254=
ENST00000558439.5:c.762A>C	ENSP00000452712.1:p.Val254=
ENST00000560508.1:c.537A>C	ENSP00000452976.1:p.Val179=
ENST00000561393.5:c.537A>C	ENSP00000452711.1:p.Val179=
ENST00000561441.5:c.762A>C	ENSP00000453112.1:p.Val254=
XM_005254264.2:c.537A>C	XP_005254321.1:p.Val179=
XM_005254264.4:c.537A>C	XP_005254321.1:p.Val179=
XM_006720447.2:c.537A>C	XP_006720510.1:p.Val179=
XM_006720447.4:c.537A>C	XP_006720510.1:p.Val179=
XM_011521408.1:c.582A>C	XP_011519710.1:p.Val194=
XM_011521409.1:c.-679A>C	XP_011519711.1:n.-679A>C
XM_017022042.2:c.-209A>C	XP_016877531.1:n.-209A>C
XR_001751183.1:n.869A>C
XR_001751184.1:n.869A>C
XR_001751185.1:n.869A>C