Canonical Allele Identifier: CA2269090869
Gene: NACA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590534T= , CM000679.2:g.61590534T= GRCh38
NC_000017.10:g.59667895T= , CM000679.1:g.59667895T= GRCh37
NC_000017.9:g.57022677T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.647A= MANE Select ENSP00000427802.1:p.Ter216=
ENST00000521764.2:c.647A= ENSP00000427802.1:p.Ter216=
NM_199290.3:c.647A= NP_954984.1:p.Ter216=
NM_199290.4:c.647A= MANE Select NP_954984.1:p.Ter216=