Canonical Allele Identifier: CA2269091027
Gene: NACA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590843T= , CM000679.2:g.61590843T= GRCh38
NC_000017.10:g.59668204T= , CM000679.1:g.59668204T= GRCh37
NC_000017.9:g.57022986T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.338A= MANE Select ENSP00000427802.1:p.Lys113=
ENST00000521764.2:c.338A= ENSP00000427802.1:p.Lys113=
NM_199290.3:c.338A= NP_954984.1:p.Lys113=
NM_199290.4:c.338A= MANE Select NP_954984.1:p.Lys113=
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