Canonical Allele Identifier: CA2637931134
Gene: HCRT HGNC NCBI

Linked Data

gnomAD v4: 17-42184661-TCCTTGCTTTGCGC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184669_42184681del , CM000679.2:g.42184669_42184681del GRCh38
NC_000017.10:g.40336687_40336699del , CM000679.1:g.40336687_40336699del GRCh37
NC_000017.9:g.37590213_37590225del NCBI36
NG_011448.1:g.5779_5791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-146_22-134del MANE Select ENSP00000293330.1:n.22-146_22-134del
NM_001524.1:c.22-146_22-134del MANE Select NP_001515.1:n.22-146_22-134del
Search 100 bp 5'
Search 100 bp 3'