Canonical Allele Identifier: CA386375931

Gene: APPL2

Linked Data

• MyVariant Identifiers: chr12:g.105583572A>T (hg19) ; chr12:g.105189794A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105189794A>T , CM000674.2:g.105189794A>T	GRCh38
NC_000012.11:g.105583572A>T , CM000674.1:g.105583572A>T	GRCh37
NC_000012.10:g.104107702A>T	NCBI36
NG_030419.1:g.51437T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258530.8:c.1437T>A MANE Select	ENSP00000258530.3:p.Asp479Glu
ENST00000258530.7:c.1437T>A	ENSP00000258530.3:p.Asp479Glu
ENST00000539978.6:c.1308T>A	ENSP00000444472.2:p.Asp436Glu
ENST00000547439.5:c.*722T>A	ENSP00000449410.1:n.*722T>A
ENST00000547809.5:n.1447T>A
ENST00000551662.5:c.1455T>A	ENSP00000446917.1:p.Asp485Glu
ENST00000552945.1:n.277T>A
ENST00000553109.1:c.81T>A	ENSP00000446510.1:p.Asp27Glu
NM_001251904.1:c.1455T>A	NP_001238833.1:p.Asp485Glu
NM_001251905.1:c.1308T>A	NP_001238834.1:p.Asp436Glu
NM_018171.3:c.1437T>A	NP_060641.2:p.Asp479Glu
XM_006719472.1:c.1455T>A	XP_006719535.1:p.Asp485Glu
XM_011538530.1:c.1416T>A	XP_011536832.1:p.Asp472Glu
XM_011538531.1:c.1326T>A	XP_011536833.1:p.Asp442Glu
XM_011538532.1:c.1326T>A	XP_011536834.1:p.Asp442Glu
XM_011538530.3:c.1416T>A	XP_011536832.1:p.Asp472Glu
XM_011538531.3:c.1326T>A	XP_011536833.1:p.Asp442Glu
XM_011538532.3:c.1326T>A	XP_011536834.1:p.Asp442Glu
XM_017019551.2:c.1398T>A	XP_016875040.1:p.Asp466Glu
XM_017019552.2:c.1308T>A	XP_016875041.1:p.Asp436Glu
XM_017019553.2:c.1308T>A	XP_016875042.1:p.Asp436Glu
XM_017019554.1:c.1437T>A	XP_016875043.1:p.Asp479Glu
XR_001748795.1:n.1617T>A
XR_001748796.1:n.1599T>A
NM_018171.4:c.1437T>A	NP_060641.2:p.Asp479Glu
NM_018171.5:c.1437T>A MANE Select	NP_060641.2:p.Asp479Glu
NM_001251904.2:c.1455T>A	NP_001238833.1:p.Asp485Glu
NM_001251905.2:c.1308T>A	NP_001238834.1:p.Asp436Glu