Canonical Allele Identifier: CA290665070

Gene: KRT14

Linked Data

• dbSNP Id: rs568781768
• gnomAD v3: 17-41584037-C-G
• gnomAD v4: 17-41584037-C-G
• MyVariant Identifiers: chr17:g.39740289C>G (hg19) ; chr17:g.41584037C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584037C>G , CM000679.2:g.41584037C>G	GRCh38
NC_000017.10:g.39740289C>G , CM000679.1:g.39740289C>G	GRCh37
NC_000017.9:g.36993815C>G	NCBI36
NG_008624.1:g.7859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-116G>C MANE Select	ENSP00000167586.6:n.766-116G>C
ENST00000167586.6:c.766-116G>C	ENSP00000167586.6:n.766-116G>C
ENST00000476662.1:n.216-116G>C
NM_000526.4:c.766-116G>C	NP_000517.2:n.766-116G>C
NM_000526.5:c.766-116G>C MANE Select	NP_000517.3:n.766-116G>C