Canonical Allele Identifier: CA13941828
Gene: ACTN1 HGNC NCBI

Linked Data

dbSNP Id: rs1009145

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68938736T>C , CM000676.2:g.68938736T>C GRCh38
NC_000014.8:g.69405453T>C , CM000676.1:g.69405453T>C GRCh37
NC_000014.7:g.68475206T>C NCBI36
NG_029480.1:g.45631A>G , LRG_886:g.45631A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000394419.9:c.106-13064A>G MANE Select ENSP00000377941.4:p.=
ENST00000679147.1:c.106-13064A>G ENSP00000504355.1:p.=
ENST00000193403.10:c.106-13064A>G ENSP00000193403.6:p.=
ENST00000376839.7:c.-90-13064A>G ENSP00000366035.3:p.=
ENST00000394419.8:c.106-13064A>G ENSP00000377941.4:p.=
ENST00000438964.6:c.106-13064A>G ENSP00000414272.2:p.=
ENST00000538545.6:c.106-13064A>G ENSP00000439828.2:p.=
ENST00000553370.5:c.-90-13064A>G ENSP00000450925.1:p.=
ENST00000553659.1:c.103-13064A>G ENSP00000451086.1:p.=
ENST00000553779.5:c.-91+8628A>G ENSP00000450618.1:p.=
ENST00000555616.5:c.-90-13064A>G ENSP00000450903.1:p.=
ENST00000556433.5:c.43-13064A>G ENSP00000450764.1:p.=
ENST00000556571.1:c.37-13064A>G ENSP00000452423.1:p.=
NM_001102.3:c.106-13064A>G NP_001093.1:p.=
NM_001130004.1:c.106-13064A>G , LRG_886t1:c.106-13064A>G NP_001123476.1:p.=
NM_001130005.1:c.106-13064A>G NP_001123477.1:p.=
XM_011537269.1:c.106-13064A>G XP_011535571.1:p.=
XM_011537270.1:c.43-13064A>G XP_011535572.1:p.=
XM_011537271.1:c.43-13064A>G XP_011535573.1:p.=
XM_017021722.2:c.106-13064A>G XP_016877211.1:p.=
XM_017021723.2:c.106-13064A>G XP_016877212.1:p.=
XM_017021725.1:c.43-13064A>G XP_016877214.1:p.=
XM_017021726.2:c.43-13064A>G XP_016877215.1:p.=
XM_017021727.2:c.106-13064A>G XP_016877216.1:p.=
XM_017021728.2:c.43-13064A>G XP_016877217.1:p.=
NM_001102.4:c.106-13064A>G NP_001093.1:p.=
NM_001130005.2:c.106-13064A>G NP_001123477.1:p.=
NM_001130004.2:c.106-13064A>G MANE Select NP_001123476.1:p.=