Canonical Allele Identifier: CA400784029

Gene: NACA2

Linked Data

• MyVariant Identifiers: chr17:g.59668115A>C (hg19) ; chr17:g.61590754A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61590754A>C , CM000679.2:g.61590754A>C	GRCh38
NC_000017.10:g.59668115A>C , CM000679.1:g.59668115A>C	GRCh37
NC_000017.9:g.57022897A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521764.3:c.427T>G MANE Select	ENSP00000427802.1:p.Phe143Val
ENST00000521764.2:c.427T>G	ENSP00000427802.1:p.Phe143Val
NM_199290.3:c.427T>G	NP_954984.1:p.Phe143Val
NM_199290.4:c.427T>G MANE Select	NP_954984.1:p.Phe143Val