Canonical Allele Identifier: CA500205599
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739611G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583359G>A , CM000679.2:g.41583359G>A GRCh38
NC_000017.10:g.39739611G>A , CM000679.1:g.39739611G>A GRCh37
NC_000017.9:g.36993137G>A NCBI36
NG_008624.1:g.8537C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1150C>T MANE Select ENSP00000167586.6:p.Leu384=
ENST00000167586.6:c.1150C>T ENSP00000167586.6:p.Leu384=
ENST00000441550.2:n.97C>T
ENST00000476662.1:n.600C>T
NM_000526.4:c.1150C>T NP_000517.2:p.Leu384=
NM_000526.5:c.1150C>T MANE Select NP_000517.3:p.Leu384=
Search 100 bp 5'
Search 100 bp 3'