Canonical Allele Identifier: CA400784056

Gene: NACA2

Linked Data

• MyVariant Identifiers: chr17:g.59668127C>A (hg19) ; chr17:g.61590766C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61590766C>A , CM000679.2:g.61590766C>A	GRCh38
NC_000017.10:g.59668127C>A , CM000679.1:g.59668127C>A	GRCh37
NC_000017.9:g.57022909C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521764.3:c.415G>T MANE Select	ENSP00000427802.1:p.Ala139Ser
ENST00000521764.2:c.415G>T	ENSP00000427802.1:p.Ala139Ser
NM_199290.3:c.415G>T	NP_954984.1:p.Ala139Ser
NM_199290.4:c.415G>T MANE Select	NP_954984.1:p.Ala139Ser