Canonical Allele Identifier: CA2260085290

Gene: KRT14

Linked Data

• ClinVar Variation Id: 1048027
• ClinVar RCV Id: RCV001352835
• dbSNP Id: rs1907395416

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583230C>G , CM000679.2:g.41583230C>G	GRCh38
NC_000017.10:g.39739482C>G , CM000679.1:g.39739482C>G	GRCh37
NC_000017.9:g.36993008C>G	NCBI36
NG_008624.1:g.8666G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1274+5G>C MANE Select	ENSP00000167586.6:n.1274+5G>C
ENST00000167586.6:c.1274+5G>C	ENSP00000167586.6:n.1274+5G>C
ENST00000441550.2:n.221+5G>C
NM_000526.4:c.1274+5G>C	NP_000517.2:n.1274+5G>C
NM_000526.5:c.1274+5G>C MANE Select	NP_000517.3:n.1274+5G>C