Canonical Allele Identifier: CA499992013
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586496-G-A
MyVariant Identifiers: chr17:g.39742748G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586496G>A , CM000679.2:g.41586496G>A GRCh38
NC_000017.10:g.39742748G>A , CM000679.1:g.39742748G>A GRCh37
NC_000017.9:g.36996274G>A NCBI36
NG_008624.1:g.5400C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.339C>T MANE Select ENSP00000167586.6:p.Gly113=
ENST00000167586.6:c.339C>T ENSP00000167586.6:p.Gly113=
NM_000526.4:c.339C>T NP_000517.2:p.Gly113=
NM_000526.5:c.339C>T MANE Select NP_000517.3:p.Gly113=
Search 100 bp 5'
Search 100 bp 3'