Canonical Allele Identifier: CA983758485

Gene: KRT14

Linked Data

• dbSNP Id: rs1907466259

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584629A>G , CM000679.2:g.41584629A>G	GRCh38
NC_000017.10:g.39740881A>G , CM000679.1:g.39740881A>G	GRCh37
NC_000017.9:g.36994407A>G	NCBI36
NG_008624.1:g.7267T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.609-216T>C MANE Select	ENSP00000167586.6:n.609-216T>C
ENST00000167586.6:c.609-216T>C	ENSP00000167586.6:n.609-216T>C
NM_000526.4:c.609-216T>C	NP_000517.2:n.609-216T>C
NM_000526.5:c.609-216T>C MANE Select	NP_000517.3:n.609-216T>C