Canonical Allele Identifier: CA13563767
Gene: ARCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118581619G>C , CM000673.2:g.118581619G>C GRCh38
NC_000011.9:g.118452334G>C , CM000673.1:g.118452334G>C GRCh37
NC_000011.8:g.117957544G>C NCBI36
NG_051953.1:g.14233G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264028.5:c.267+110G>C MANE Select ENSP00000264028.4:n.267+110G>C
ENST00000264028.4:c.267+110G>C ENSP00000264028.4:n.267+110G>C
ENST00000359415.8:c.390+110G>C ENSP00000352385.4:n.390+110G>C
ENST00000392859.7:c.4-1560G>C ENSP00000376599.3:n.4-1560G>C
ENST00000534182.2:c.159+218G>C ENSP00000431676.1:n.159+218G>C
ENST00000614498.4:c.267+110G>C ENSP00000482114.1:n.267+110G>C
NM_001142281.1:c.4-1560G>C NP_001135753.1:n.4-1560G>C
NM_001655.4:c.267+110G>C NP_001646.2:n.267+110G>C
XM_005271542.2:c.267+110G>C XP_005271599.1:n.267+110G>C
XM_005271542.4:c.267+110G>C XP_005271599.1:n.267+110G>C
NM_001655.5:c.267+110G>C MANE Select NP_001646.2:n.267+110G>C
NM_001142281.2:c.4-1560G>C NP_001135753.1:n.4-1560G>C