Canonical Allele Identifier: CA2323741302
Gene: NACC1 HGNC NCBI

Linked Data

dbSNP Id: rs2019682797
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13135115del , CM000681.2:g.13135115del GRCh38
NC_000019.9:g.13245929del , CM000681.1:g.13245929del GRCh37
NC_000019.8:g.13106929del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000586171.3:c.-8-85del ENSP00000467120.2:n.-8-85del
ENST00000700232.1:c.-8-85del ENSP00000514870.1:n.-8-85del
ENST00000292431.5:c.-8-85del MANE Select ENSP00000292431.3:n.-8-85del
ENST00000586171.2:c.-8-85del ENSP00000467120.1:n.-8-85del
ENST00000292431.4:c.-8-85del ENSP00000292431.3:n.-8-85del
ENST00000586171.1:c.-8-85del ENSP00000467120.1:n.-8-85del
NM_052876.3:c.-8-85del NP_443108.1:n.-8-85del
XM_005259721.2:c.-8-85del XP_005259778.1:n.-8-85del
XM_005259721.3:c.-8-85del XP_005259778.1:n.-8-85del
NM_052876.4:c.-8-85del MANE Select NP_443108.1:n.-8-85del
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