Canonical Allele Identifier: CA386375984

Gene: APPL2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105189803T>G , CM000674.2:g.105189803T>G	GRCh38
NC_000012.11:g.105583581T>G , CM000674.1:g.105583581T>G	GRCh37
NC_000012.10:g.104107711T>G	NCBI36
NG_030419.1:g.51428A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258530.8:c.1428A>C MANE Select	ENSP00000258530.3:p.Glu476Asp
ENST00000258530.7:c.1428A>C	ENSP00000258530.3:p.Glu476Asp
ENST00000539978.6:c.1299A>C	ENSP00000444472.2:p.Glu433Asp
ENST00000547439.5:c.*713A>C	ENSP00000449410.1:n.*713A>C
ENST00000547809.5:n.1438A>C
ENST00000551662.5:c.1446A>C	ENSP00000446917.1:p.Glu482Asp
ENST00000552945.1:n.268A>C
ENST00000553109.1:c.72A>C	ENSP00000446510.1:p.Glu24Asp
NM_001251904.1:c.1446A>C	NP_001238833.1:p.Glu482Asp
NM_001251905.1:c.1299A>C	NP_001238834.1:p.Glu433Asp
NM_018171.3:c.1428A>C	NP_060641.2:p.Glu476Asp
XM_006719472.1:c.1446A>C	XP_006719535.1:p.Glu482Asp
XM_011538530.1:c.1407A>C	XP_011536832.1:p.Glu469Asp
XM_011538531.1:c.1317A>C	XP_011536833.1:p.Glu439Asp
XM_011538532.1:c.1317A>C	XP_011536834.1:p.Glu439Asp
XM_011538530.3:c.1407A>C	XP_011536832.1:p.Glu469Asp
XM_011538531.3:c.1317A>C	XP_011536833.1:p.Glu439Asp
XM_011538532.3:c.1317A>C	XP_011536834.1:p.Glu439Asp
XM_017019551.2:c.1389A>C	XP_016875040.1:p.Glu463Asp
XM_017019552.2:c.1299A>C	XP_016875041.1:p.Glu433Asp
XM_017019553.2:c.1299A>C	XP_016875042.1:p.Glu433Asp
XM_017019554.1:c.1428A>C	XP_016875043.1:p.Glu476Asp
XR_001748795.1:n.1608A>C
XR_001748796.1:n.1590A>C
NM_018171.4:c.1428A>C	NP_060641.2:p.Glu476Asp
NM_018171.5:c.1428A>C MANE Select	NP_060641.2:p.Glu476Asp
NM_001251904.2:c.1446A>C	NP_001238833.1:p.Glu482Asp
NM_001251905.2:c.1299A>C	NP_001238834.1:p.Glu433Asp