Canonical Allele Identifier: CA400784048

Gene: NACA2

Linked Data

• gnomAD v4: 17-61590762-G-C
• MyVariant Identifiers: chr17:g.59668123G>C (hg19) ; chr17:g.61590762G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61590762G>C , CM000679.2:g.61590762G>C	GRCh38
NC_000017.10:g.59668123G>C , CM000679.1:g.59668123G>C	GRCh37
NC_000017.9:g.57022905G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521764.3:c.419C>G MANE Select	ENSP00000427802.1:p.Ala140Gly
ENST00000521764.2:c.419C>G	ENSP00000427802.1:p.Ala140Gly
NM_199290.3:c.419C>G	NP_954984.1:p.Ala140Gly
NM_199290.4:c.419C>G MANE Select	NP_954984.1:p.Ala140Gly