Canonical Allele Identifier: CA399483443
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs566001198

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586713C>G , CM000679.2:g.41586713C>G GRCh38
NC_000017.10:g.39742965C>G , CM000679.1:g.39742965C>G GRCh37
NC_000017.9:g.36996491C>G NCBI36
NG_008624.1:g.5183G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.122G>C MANE Select ENSP00000167586.6:p.Arg41Pro
ENST00000167586.6:c.122G>C ENSP00000167586.6:p.Arg41Pro
NM_000526.4:c.122G>C NP_000517.2:p.Arg41Pro
NM_000526.5:c.122G>C MANE Select NP_000517.3:p.Arg41Pro