Canonical Allele Identifier: CA626215459
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1250983467
gnomAD v2: 17-39743086-TG-T
gnomAD v4: 17-41586834-TG-T
MyVariant Identifiers: chr17:g.39743087del (hg19) chr17:g.41586835del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586836del , CM000679.2:g.41586836del GRCh38
NC_000017.10:g.39743088del , CM000679.1:g.39743088del GRCh37
NC_000017.9:g.36996614del NCBI36
NG_008624.1:g.5061del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-1del MANE Select ENSP00000167586.6:n.-1del
ENST00000167586.6:c.-1del ENSP00000167586.6:n.-1del
NM_000526.4:c.-1del NP_000517.2:n.-1del
NM_000526.5:c.-1del MANE Select NP_000517.3:n.-1del
Search 100 bp 5'
Search 100 bp 3'