Canonical Allele Identifier: CA1729043540
Gene: ARPC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99360257C= , CM000669.2:g.99360257C= GRCh38
NC_000007.13:g.98957880C= , CM000669.1:g.98957880C= GRCh37
NC_000007.12:g.98795816C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006409.4:c.983+519C= MANE Select NP_006400.2:n.983+519C=
ENST00000262942.10:c.983+519C= MANE Select ENSP00000262942.5:n.983+519C=
NM_001190996.1:c.941+519C= NP_001177925.1:n.941+519C=
NM_001190996.2:c.941+519C= NP_001177925.1:n.941+519C=
NM_006409.3:c.983+519C= NP_006400.2:n.983+519C=
ENST00000262942.9:c.983+519C= ENSP00000262942.5:n.983+519C=
ENST00000432786.5:c.*142+519C= ENSP00000408711.1:n.*142+519C=
ENST00000441989.6:c.*1005+519C= ENSP00000412879.1:n.*1005+519C=
ENST00000463009.1:n.304+519C=
ENST00000638617.1:c.983+519C= ENSP00000491073.1:n.983+519C=