Canonical Allele Identifier: CA15487549

Gene: ARPC1A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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