Canonical Allele Identifier: CA305552566
Gene: NACC1 HGNC NCBI

Linked Data

dbSNP Id: rs10408126

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13135154C>T , CM000681.2:g.13135154C>T GRCh38
NC_000019.9:g.13245968C>T , CM000681.1:g.13245968C>T GRCh37
NC_000019.8:g.13106968C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000586171.3:c.-8-46C>T ENSP00000467120.2:n.-8-46C>T
ENST00000700232.1:c.-8-46C>T ENSP00000514870.1:n.-8-46C>T
ENST00000292431.5:c.-8-46C>T MANE Select ENSP00000292431.3:n.-8-46C>T
ENST00000586171.2:c.-8-46C>T ENSP00000467120.1:n.-8-46C>T
ENST00000292431.4:c.-8-46C>T ENSP00000292431.3:n.-8-46C>T
ENST00000586171.1:c.-8-46C>T ENSP00000467120.1:n.-8-46C>T
NM_052876.3:c.-8-46C>T NP_443108.1:n.-8-46C>T
XM_005259721.2:c.-8-46C>T XP_005259778.1:n.-8-46C>T
XM_005259721.3:c.-8-46C>T XP_005259778.1:n.-8-46C>T
NM_052876.4:c.-8-46C>T MANE Select NP_443108.1:n.-8-46C>T