Canonical Allele Identifier: CA399482560
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1252105996

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586473T>C , CM000679.2:g.41586473T>C GRCh38
NC_000017.10:g.39742725T>C , CM000679.1:g.39742725T>C GRCh37
NC_000017.9:g.36996251T>C NCBI36
NG_008624.1:g.5423A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.362A>G MANE Select ENSP00000167586.6:p.Asn121Ser
ENST00000167586.6:c.362A>G ENSP00000167586.6:p.Asn121Ser
NM_000526.4:c.362A>G NP_000517.2:p.Asn121Ser
NM_000526.5:c.362A>G MANE Select NP_000517.3:p.Asn121Ser