Canonical Allele Identifier: CA2323741779
Gene: NACC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13136187_13136188delinsCA , CM000681.2:g.13136187_13136188delinsCA GRCh38
NC_000019.9:g.13247001_13247002delinsCA , CM000681.1:g.13247001_13247002delinsCA GRCh37
NC_000019.8:g.13108001_13108002delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000586171.3:c.946+34_946+35delinsCA ENSP00000467120.2:n.946+34_946+35delinsCA
ENST00000700232.1:c.946+34_946+35delinsCA ENSP00000514870.1:n.946+34_946+35delinsCA
ENST00000292431.5:c.946+34_946+35delinsCA MANE Select ENSP00000292431.3:n.946+34_946+35delinsCA
ENST00000292431.4:c.946+34_946+35delinsCA ENSP00000292431.3:n.946+34_946+35delinsCA
NM_052876.3:c.946+34_946+35delinsCA NP_443108.1:n.946+34_946+35delinsCA
XM_005259721.2:c.946+34_946+35delinsCA XP_005259778.1:n.946+34_946+35delinsCA
XM_005259721.3:c.946+34_946+35delinsCA XP_005259778.1:n.946+34_946+35delinsCA
NM_052876.4:c.946+34_946+35delinsCA MANE Select NP_443108.1:n.946+34_946+35delinsCA