Canonical Allele Identifier: CA2323741356
Gene: NACC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13135207C= , CM000681.2:g.13135207C= GRCh38
NC_000019.9:g.13246021C= , CM000681.1:g.13246021C= GRCh37
NC_000019.8:g.13107021C= NCBI36

Transcript Alleles

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