Canonical Allele Identifier: CA399483406
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586707-G-T
MyVariant Identifiers: chr17:g.39742959G>T (hg19) chr17:g.41586707G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586707G>T , CM000679.2:g.41586707G>T GRCh38
NC_000017.10:g.39742959G>T , CM000679.1:g.39742959G>T GRCh37
NC_000017.9:g.36996485G>T NCBI36
NG_008624.1:g.5189C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.128C>A MANE Select ENSP00000167586.6:p.Pro43His
ENST00000167586.6:c.128C>A ENSP00000167586.6:p.Pro43His
NM_000526.4:c.128C>A NP_000517.2:p.Pro43His
NM_000526.5:c.128C>A MANE Select NP_000517.3:p.Pro43His
Search 100 bp 5'
Search 100 bp 3'