Canonical Allele Identifier: CA399482823

Gene: KRT14

Linked Data

• dbSNP Id: rs1907535014
• MyVariant Identifiers: chr17:g.39742797C>G (hg19) ; chr17:g.41586545C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586545C>G , CM000679.2:g.41586545C>G	GRCh38
NC_000017.10:g.39742797C>G , CM000679.1:g.39742797C>G	GRCh37
NC_000017.9:g.36996323C>G	NCBI36
NG_008624.1:g.5351G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.290G>C MANE Select	ENSP00000167586.6:p.Gly97Ala
ENST00000167586.6:c.290G>C	ENSP00000167586.6:p.Gly97Ala
NM_000526.4:c.290G>C	NP_000517.2:p.Gly97Ala
NM_000526.5:c.290G>C MANE Select	NP_000517.3:p.Gly97Ala