Canonical Allele Identifier: CA386376489

Gene: APPL2

Linked Data

• MyVariant Identifiers: chr12:g.105583824G>C (hg19) ; chr12:g.105190046G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105190046G>C , CM000674.2:g.105190046G>C	GRCh38
NC_000012.11:g.105583824G>C , CM000674.1:g.105583824G>C	GRCh37
NC_000012.10:g.104107954G>C	NCBI36
NG_030419.1:g.51185C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258530.8:c.1351C>G MANE Select	ENSP00000258530.3:p.Gln451Glu
ENST00000258530.7:c.1351C>G	ENSP00000258530.3:p.Gln451Glu
ENST00000539978.6:c.1222C>G	ENSP00000444472.2:p.Gln408Glu
ENST00000547439.5:c.*636C>G	ENSP00000449410.1:n.*636C>G
ENST00000547809.5:n.1361C>G
ENST00000551662.5:c.1369C>G	ENSP00000446917.1:p.Gln457Glu
ENST00000552945.1:n.126C>G
NM_001251904.1:c.1369C>G	NP_001238833.1:p.Gln457Glu
NM_001251905.1:c.1222C>G	NP_001238834.1:p.Gln408Glu
NM_018171.3:c.1351C>G	NP_060641.2:p.Gln451Glu
XM_006719472.1:c.1369C>G	XP_006719535.1:p.Gln457Glu
XM_011538530.1:c.1330C>G	XP_011536832.1:p.Gln444Glu
XM_011538531.1:c.1240C>G	XP_011536833.1:p.Gln414Glu
XM_011538532.1:c.1240C>G	XP_011536834.1:p.Gln414Glu
XM_011538530.3:c.1330C>G	XP_011536832.1:p.Gln444Glu
XM_011538531.3:c.1240C>G	XP_011536833.1:p.Gln414Glu
XM_011538532.3:c.1240C>G	XP_011536834.1:p.Gln414Glu
XM_017019551.2:c.1312C>G	XP_016875040.1:p.Gln438Glu
XM_017019552.2:c.1222C>G	XP_016875041.1:p.Gln408Glu
XM_017019553.2:c.1222C>G	XP_016875042.1:p.Gln408Glu
XM_017019554.1:c.1351C>G	XP_016875043.1:p.Gln451Glu
XR_001748795.1:n.1531C>G
XR_001748796.1:n.1513C>G
NM_018171.4:c.1351C>G	NP_060641.2:p.Gln451Glu
NM_018171.5:c.1351C>G MANE Select	NP_060641.2:p.Gln451Glu
NM_001251904.2:c.1369C>G	NP_001238833.1:p.Gln457Glu
NM_001251905.2:c.1222C>G	NP_001238834.1:p.Gln408Glu