Canonical Allele Identifier: CA499989885
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740601G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584349G>A , CM000679.2:g.41584349G>A GRCh38
NC_000017.10:g.39740601G>A , CM000679.1:g.39740601G>A GRCh37
NC_000017.9:g.36994127G>A NCBI36
NG_008624.1:g.7547C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.673C>T MANE Select ENSP00000167586.6:p.Leu225=
ENST00000167586.6:c.673C>T ENSP00000167586.6:p.Leu225=
ENST00000476662.1:n.123C>T
NM_000526.4:c.673C>T NP_000517.2:p.Leu225=
NM_000526.5:c.673C>T MANE Select NP_000517.3:p.Leu225=
Search 100 bp 5'
Search 100 bp 3'