Canonical Allele Identifier: CA500205591
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739606G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583354G>C , CM000679.2:g.41583354G>C GRCh38
NC_000017.10:g.39739606G>C , CM000679.1:g.39739606G>C GRCh37
NC_000017.9:g.36993132G>C NCBI36
NG_008624.1:g.8542C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1155C>G MANE Select ENSP00000167586.6:p.Ala385=
ENST00000167586.6:c.1155C>G ENSP00000167586.6:p.Ala385=
ENST00000441550.2:n.102C>G
ENST00000476662.1:n.605C>G
NM_000526.4:c.1155C>G NP_000517.2:p.Ala385=
NM_000526.5:c.1155C>G MANE Select NP_000517.3:p.Ala385=