Canonical Allele Identifier: CA500205382
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41583599-C-G
MyVariant Identifiers: chr17:g.39739851C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583599C>G , CM000679.2:g.41583599C>G GRCh38
NC_000017.10:g.39739851C>G , CM000679.1:g.39739851C>G GRCh37
NC_000017.9:g.36993377C>G NCBI36
NG_008624.1:g.8297G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1005G>C MANE Select ENSP00000167586.6:p.Arg335=
ENST00000167586.6:c.1005G>C ENSP00000167586.6:p.Arg335=
ENST00000476662.1:n.455G>C
NM_000526.4:c.1005G>C NP_000517.2:p.Arg335=
NM_000526.5:c.1005G>C MANE Select NP_000517.3:p.Arg335=
Search 100 bp 5'
Search 100 bp 3'