Canonical Allele Identifier: CA399474923

Gene: KRT14

Linked Data

• MyVariant Identifiers: chr17:g.39739361G>T (hg19) ; chr17:g.41583109G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583109G>T , CM000679.2:g.41583109G>T	GRCh38
NC_000017.10:g.39739361G>T , CM000679.1:g.39739361G>T	GRCh37
NC_000017.9:g.36992887G>T	NCBI36
NG_008624.1:g.8787C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1306C>A MANE Select	ENSP00000167586.6:p.Gln436Lys
ENST00000167586.6:c.1306C>A	ENSP00000167586.6:p.Gln436Lys
ENST00000441550.2:n.253C>A
NM_000526.4:c.1306C>A	NP_000517.2:p.Gln436Lys
NM_000526.5:c.1306C>A MANE Select	NP_000517.3:p.Gln436Lys