Canonical Allele Identifier: CA2260086753
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907519633

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586292T>C , CM000679.2:g.41586292T>C GRCh38
NC_000017.10:g.39742544T>C , CM000679.1:g.39742544T>C GRCh37
NC_000017.9:g.36996070T>C NCBI36
NG_008624.1:g.5604A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.525+18A>G MANE Select ENSP00000167586.6:n.525+18A>G
ENST00000167586.6:c.525+18A>G ENSP00000167586.6:n.525+18A>G
NM_000526.4:c.525+18A>G NP_000517.2:n.525+18A>G
NM_000526.5:c.525+18A>G MANE Select NP_000517.3:n.525+18A>G