Canonical Allele Identifier: CA2639152785
Gene: NACA2 HGNC NCBI

Linked Data

gnomAD v4: 17-61590677-CTCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590680_61590682del , CM000679.2:g.61590680_61590682del GRCh38
NC_000017.10:g.59668041_59668043del , CM000679.1:g.59668041_59668043del GRCh37
NC_000017.9:g.57022823_57022825del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.501_503del MANE Select ENSP00000427802.1:p.Glu168del
ENST00000521764.2:c.501_503del ENSP00000427802.1:p.Glu168del
NM_199290.3:c.501_503del NP_954984.1:p.Glu168del
NM_199290.4:c.501_503del MANE Select NP_954984.1:p.Glu168del
Search 100 bp 5'
Search 100 bp 3'