Canonical Allele Identifier: CA481640139

Gene: APPL2

Linked Data

• MyVariant Identifiers: chr12:g.105583560T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105189782T>A , CM000674.2:g.105189782T>A	GRCh38
NC_000012.11:g.105583560T>A , CM000674.1:g.105583560T>A	GRCh37
NC_000012.10:g.104107690T>A	NCBI36
NG_030419.1:g.51449A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258530.8:c.1449A>T MANE Select	ENSP00000258530.3:p.Pro483=
ENST00000258530.7:c.1449A>T	ENSP00000258530.3:p.Pro483=
ENST00000539978.6:c.1320A>T	ENSP00000444472.2:p.Pro440=
ENST00000547439.5:c.*734A>T	ENSP00000449410.1:n.*734A>T
ENST00000547809.5:n.1459A>T
ENST00000551662.5:c.1467A>T	ENSP00000446917.1:p.Pro489=
ENST00000552945.1:n.289A>T
ENST00000553109.1:c.93A>T	ENSP00000446510.1:p.Pro31=
NM_001251904.1:c.1467A>T	NP_001238833.1:p.Pro489=
NM_001251905.1:c.1320A>T	NP_001238834.1:p.Pro440=
NM_018171.3:c.1449A>T	NP_060641.2:p.Pro483=
XM_006719472.1:c.1467A>T	XP_006719535.1:p.Pro489=
XM_011538530.1:c.1428A>T	XP_011536832.1:p.Pro476=
XM_011538531.1:c.1338A>T	XP_011536833.1:p.Pro446=
XM_011538532.1:c.1338A>T	XP_011536834.1:p.Pro446=
XM_011538530.3:c.1428A>T	XP_011536832.1:p.Pro476=
XM_011538531.3:c.1338A>T	XP_011536833.1:p.Pro446=
XM_011538532.3:c.1338A>T	XP_011536834.1:p.Pro446=
XM_017019551.2:c.1410A>T	XP_016875040.1:p.Pro470=
XM_017019552.2:c.1320A>T	XP_016875041.1:p.Pro440=
XM_017019553.2:c.1320A>T	XP_016875042.1:p.Pro440=
XM_017019554.1:c.1449A>T	XP_016875043.1:p.Pro483=
XR_001748795.1:n.1629A>T
XR_001748796.1:n.1611A>T
NM_018171.4:c.1449A>T	NP_060641.2:p.Pro483=
NM_018171.5:c.1449A>T MANE Select	NP_060641.2:p.Pro483=
NM_001251904.2:c.1467A>T	NP_001238833.1:p.Pro489=
NM_001251905.2:c.1320A>T	NP_001238834.1:p.Pro440=