Canonical Allele Identifier: CA2637836126
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41584255-ACCT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584260_41584262del , CM000679.2:g.41584260_41584262del GRCh38
NC_000017.10:g.39740512_39740514del , CM000679.1:g.39740512_39740514del GRCh37
NC_000017.9:g.36994038_36994040del NCBI36
NG_008624.1:g.7638_7640del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.764_765+1del
ENST00000167586.6:c.764_765+1del
ENST00000476662.1:n.214_215+1del
NM_000526.4:c.764_765+1del
NM_000526.5:c.764_765+1del
Search 100 bp 5'
Search 100 bp 3'