Canonical Allele Identifier: CA6306322
Gene: ARCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118600708T>C , CM000673.2:g.118600708T>C GRCh38
NC_000011.9:g.118471423T>C , CM000673.1:g.118471423T>C GRCh37
NC_000011.8:g.117976633T>C NCBI36
NG_051953.1:g.33322T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264028.5:c.1530T>C MANE Select ENSP00000264028.4:p.Ile510=
ENST00000264028.4:c.1530T>C ENSP00000264028.4:p.Ile510=
ENST00000359415.8:c.1653T>C ENSP00000352385.4:p.Ile551=
ENST00000392859.7:c.1266T>C ENSP00000376599.3:p.Ile422=
ENST00000534182.2:c.160-928T>C ENSP00000431676.1:n.160-928T>C
ENST00000614498.4:c.509-614T>C ENSP00000482114.1:n.509-614T>C
NM_001142281.1:c.1266T>C NP_001135753.1:p.Ile422=
NM_001655.4:c.1530T>C NP_001646.2:p.Ile510=
XM_005271542.2:c.*71T>C XP_005271599.1:n.*71T>C
XM_005271542.4:c.*71T>C XP_005271599.1:n.*71T>C
NM_001655.5:c.1530T>C MANE Select NP_001646.2:p.Ile510=
NM_001142281.2:c.1266T>C NP_001135753.1:p.Ile422=