Canonical Allele Identifier: CA2576267729

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583088T>A , CM000679.2:g.41583088T>A	GRCh38
NC_000017.10:g.39739340T>A , CM000679.1:g.39739340T>A	GRCh37
NC_000017.9:g.36992866T>A	NCBI36
NG_008624.1:g.8808A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.1321+6A>T MANE Select	ENSP00000167586.6:n.1321+6A>T
ENST00000167586.6:c.1321+6A>T	ENSP00000167586.6:n.1321+6A>T
ENST00000441550.2:n.274A>T
NM_000526.4:c.1321+6A>T	NP_000517.2:n.1321+6A>T
NM_000526.5:c.1321+6A>T MANE Select	NP_000517.3:n.1321+6A>T