Canonical Allele Identifier: CA2323741508
Gene: NACC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13135534C= , CM000681.2:g.13135534C= GRCh38
NC_000019.9:g.13246348C= , CM000681.1:g.13246348C= GRCh37
NC_000019.8:g.13107348C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000586171.3:c.327C= ENSP00000467120.2:p.Ile109=
ENST00000700232.1:c.327C= ENSP00000514870.1:p.Ile109=
ENST00000292431.5:c.327C= MANE Select ENSP00000292431.3:p.Ile109=
ENST00000586171.2:c.327C= ENSP00000467120.1:p.Ile109=
ENST00000292431.4:c.327C= ENSP00000292431.3:p.Ile109=
ENST00000586171.1:c.327C= ENSP00000467120.1:p.Ile109=
NM_052876.3:c.327C= NP_443108.1:p.Ile109=
XM_005259721.2:c.327C= XP_005259778.1:p.Ile109=
XM_005259721.3:c.327C= XP_005259778.1:p.Ile109=
NM_052876.4:c.327C= MANE Select NP_443108.1:p.Ile109=