Canonical Allele Identifier: CA627153529
Gene: NACA2 HGNC NCBI

Linked Data

dbSNP Id: rs1340371131
gnomAD v2: 17-59667882-GC-G
gnomAD v4: 17-61590521-GC-G
MyVariant Identifiers: chr17:g.59667883del (hg19) chr17:g.61590522del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61590522del , CM000679.2:g.61590522del GRCh38
NC_000017.10:g.59667883del , CM000679.1:g.59667883del GRCh37
NC_000017.9:g.57022665del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521764.3:c.*11del MANE Select ENSP00000427802.1:n.*11del
ENST00000521764.2:c.*11del ENSP00000427802.1:n.*11del
NM_199290.3:c.*11del NP_954984.1:n.*11del
NM_199290.4:c.*11del MANE Select NP_954984.1:n.*11del
Search 100 bp 5'
Search 100 bp 3'