Canonical Allele Identifier: CA2323741768
Gene: NACC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13136166C= , CM000681.2:g.13136166C= GRCh38
NC_000019.9:g.13246980C= , CM000681.1:g.13246980C= GRCh37
NC_000019.8:g.13107980C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000586171.3:c.946+13C= ENSP00000467120.2:n.946+13C=
ENST00000700232.1:c.946+13C= ENSP00000514870.1:n.946+13C=
ENST00000292431.5:c.946+13C= MANE Select ENSP00000292431.3:n.946+13C=
ENST00000292431.4:c.946+13C= ENSP00000292431.3:n.946+13C=
NM_052876.3:c.946+13C= NP_443108.1:n.946+13C=
XM_005259721.2:c.946+13C= XP_005259778.1:n.946+13C=
XM_005259721.3:c.946+13C= XP_005259778.1:n.946+13C=
NM_052876.4:c.946+13C= MANE Select NP_443108.1:n.946+13C=
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