Canonical Allele Identifier: CA500205832
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39743009G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586757G>T , CM000679.2:g.41586757G>T GRCh38
NC_000017.10:g.39743009G>T , CM000679.1:g.39743009G>T GRCh37
NC_000017.9:g.36996535G>T NCBI36
NG_008624.1:g.5139C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.78C>A MANE Select ENSP00000167586.6:p.Gly26=
ENST00000167586.6:c.78C>A ENSP00000167586.6:p.Gly26=
NM_000526.4:c.78C>A NP_000517.2:p.Gly26=
NM_000526.5:c.78C>A MANE Select NP_000517.3:p.Gly26=
Search 100 bp 5'
Search 100 bp 3'