Canonical Allele Identifier: CA399483446
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs536753971

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586714G>C , CM000679.2:g.41586714G>C GRCh38
NC_000017.10:g.39742966G>C , CM000679.1:g.39742966G>C GRCh37
NC_000017.9:g.36996492G>C NCBI36
NG_008624.1:g.5182C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.121C>G MANE Select ENSP00000167586.6:p.Arg41Gly
ENST00000167586.6:c.121C>G ENSP00000167586.6:p.Arg41Gly
NM_000526.4:c.121C>G NP_000517.2:p.Arg41Gly
NM_000526.5:c.121C>G MANE Select NP_000517.3:p.Arg41Gly