Canonical Allele Identifier: CA2618968354
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814385-C-CCCAGG
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814386_52814387insCAGGC , CM000674.2:g.52814386_52814387insCAGGC GRCh38
NC_000012.11:g.53208170_53208171insCAGGC , CM000674.1:g.53208170_53208171insCAGGC GRCh37
NC_000012.10:g.51494437_51494438insCAGGC NCBI36
NG_007380.1:g.5166_5167insCCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-328_-327insCCTGG ENSP00000448220.1:n.-328_-327insCCTGG
Search 100 bp 5'
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