Canonical Allele Identifier: CA2269090953
Gene: NACA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590703G= , CM000679.2:g.61590703G= GRCh38
NC_000017.10:g.59668064G= , CM000679.1:g.59668064G= GRCh37
NC_000017.9:g.57022846G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.478C= MANE Select ENSP00000427802.1:p.Pro160=
ENST00000521764.2:c.478C= ENSP00000427802.1:p.Pro160=
NM_199290.3:c.478C= NP_954984.1:p.Pro160=
NM_199290.4:c.478C= MANE Select NP_954984.1:p.Pro160=