Canonical Allele Identifier: CA501351491
Gene: NACA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.59668128T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590767T>A , CM000679.2:g.61590767T>A GRCh38
NC_000017.10:g.59668128T>A , CM000679.1:g.59668128T>A GRCh37
NC_000017.9:g.57022910T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.414A>T MANE Select ENSP00000427802.1:p.Ala138=
ENST00000521764.2:c.414A>T ENSP00000427802.1:p.Ala138=
NM_199290.3:c.414A>T NP_954984.1:p.Ala138=
NM_199290.4:c.414A>T MANE Select NP_954984.1:p.Ala138=