Canonical Allele Identifier: CA2060497558
Gene: APPL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105189860C>G , CM000674.2:g.105189860C>G GRCh38
NC_000012.11:g.105583638C>G , CM000674.1:g.105583638C>G GRCh37
NC_000012.10:g.104107768C>G NCBI36
NG_030419.1:g.51371G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258530.8:c.1407-36G>C MANE Select ENSP00000258530.3:n.1407-36G>C
ENST00000258530.7:c.1407-36G>C ENSP00000258530.3:n.1407-36G>C
ENST00000539978.6:c.1278-36G>C ENSP00000444472.2:n.1278-36G>C
ENST00000547439.5:c.*692-36G>C ENSP00000449410.1:n.*692-36G>C
ENST00000547809.5:n.1417-36G>C
ENST00000551662.5:c.1425-36G>C ENSP00000446917.1:n.1425-36G>C
ENST00000552945.1:n.211G>C
ENST00000553109.1:n.51-36G>C ENSP00000446510.1:n.51-36G>C
NM_001251904.1:c.1425-36G>C NP_001238833.1:n.1425-36G>C
NM_001251905.1:c.1278-36G>C NP_001238834.1:n.1278-36G>C
NM_018171.3:c.1407-36G>C NP_060641.2:n.1407-36G>C
XM_006719472.1:c.1425-36G>C XP_006719535.1:n.1425-36G>C
XM_011538530.1:c.1386-36G>C XP_011536832.1:n.1386-36G>C
XM_011538531.1:c.1296-36G>C XP_011536833.1:n.1296-36G>C
XM_011538532.1:c.1296-36G>C XP_011536834.1:n.1296-36G>C
XM_011538530.3:c.1386-36G>C XP_011536832.1:n.1386-36G>C
XM_011538531.3:c.1296-36G>C XP_011536833.1:n.1296-36G>C
XM_011538532.3:c.1296-36G>C XP_011536834.1:n.1296-36G>C
XM_017019551.2:c.1368-36G>C XP_016875040.1:n.1368-36G>C
XM_017019552.2:c.1278-36G>C XP_016875041.1:n.1278-36G>C
XM_017019553.2:c.1278-36G>C XP_016875042.1:n.1278-36G>C
XM_017019554.1:c.1407-36G>C XP_016875043.1:n.1407-36G>C
XR_001748795.1:n.1587-36G>C
XR_001748796.1:n.1569-36G>C
NM_018171.4:c.1407-36G>C NP_060641.2:n.1407-36G>C
NM_018171.5:c.1407-36G>C MANE Select NP_060641.2:n.1407-36G>C
NM_001251904.2:c.1425-36G>C NP_001238833.1:n.1425-36G>C
NM_001251905.2:c.1278-36G>C NP_001238834.1:n.1278-36G>C