Canonical Allele Identifier: CA6759514

Gene: APPL2

Linked Data

• dbSNP Id: rs765693162
• ExAC: 12:105583503 T / C
• gnomAD v2: 12-105583503-T-C
• gnomAD v4: 12-105189725-T-C
• MyVariant Identifiers: chr12:g.105583503T>C (hg19) ; chr12:g.105189725T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105189725T>C , CM000674.2:g.105189725T>C	GRCh38
NC_000012.11:g.105583503T>C , CM000674.1:g.105583503T>C	GRCh37
NC_000012.10:g.104107633T>C	NCBI36
NG_030419.1:g.51506A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258530.8:c.1459+47A>G MANE Select	ENSP00000258530.3:n.1459+47A>G
ENST00000258530.7:c.1459+47A>G	ENSP00000258530.3:n.1459+47A>G
ENST00000539978.6:c.1330+47A>G	ENSP00000444472.2:n.1330+47A>G
ENST00000547439.5:c.*744+47A>G	ENSP00000449410.1:n.*744+47A>G
ENST00000547809.5:n.1469+47A>G
ENST00000551662.5:c.1477+47A>G	ENSP00000446917.1:n.1477+47A>G
ENST00000552945.1:n.299+47A>G
ENST00000553109.1:c.103+47A>G	ENSP00000446510.1:n.103+47A>G
NM_001251904.1:c.1477+47A>G	NP_001238833.1:n.1477+47A>G
NM_001251905.1:c.1330+47A>G	NP_001238834.1:n.1330+47A>G
NM_018171.3:c.1459+47A>G	NP_060641.2:n.1459+47A>G
XM_006719472.1:c.1477+47A>G	XP_006719535.1:n.1477+47A>G
XM_011538530.1:c.1438+47A>G	XP_011536832.1:n.1438+47A>G
XM_011538531.1:c.1348+47A>G	XP_011536833.1:n.1348+47A>G
XM_011538532.1:c.1348+47A>G	XP_011536834.1:n.1348+47A>G
XM_011538530.3:c.1438+47A>G	XP_011536832.1:n.1438+47A>G
XM_011538531.3:c.1348+47A>G	XP_011536833.1:n.1348+47A>G
XM_011538532.3:c.1348+47A>G	XP_011536834.1:n.1348+47A>G
XM_017019551.2:c.1420+47A>G	XP_016875040.1:n.1420+47A>G
XM_017019552.2:c.1330+47A>G	XP_016875041.1:n.1330+47A>G
XM_017019553.2:c.1330+47A>G	XP_016875042.1:n.1330+47A>G
XM_017019554.1:c.1459+47A>G	XP_016875043.1:n.1459+47A>G
XR_001748795.1:n.1639+47A>G
XR_001748796.1:n.1621+47A>G
NM_018171.4:c.1459+47A>G	NP_060641.2:n.1459+47A>G
NM_018171.5:c.1459+47A>G MANE Select	NP_060641.2:n.1459+47A>G
NM_001251904.2:c.1477+47A>G	NP_001238833.1:n.1477+47A>G
NM_001251905.2:c.1330+47A>G	NP_001238834.1:n.1330+47A>G