Canonical Allele Identifier: CA500205619
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739621C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583369C>A , CM000679.2:g.41583369C>A GRCh38
NC_000017.10:g.39739621C>A , CM000679.1:g.39739621C>A GRCh37
NC_000017.9:g.36993147C>A NCBI36
NG_008624.1:g.8527G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1140G>T MANE Select ENSP00000167586.6:p.Val380=
ENST00000167586.6:c.1140G>T ENSP00000167586.6:p.Val380=
ENST00000441550.2:n.87G>T
ENST00000476662.1:n.590G>T
NM_000526.4:c.1140G>T NP_000517.2:p.Val380=
NM_000526.5:c.1140G>T MANE Select NP_000517.3:p.Val380=
Search 100 bp 5'
Search 100 bp 3'