Canonical Allele Identifier: CA8562426
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs763910781

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583181G>A , CM000679.2:g.41583181G>A GRCh38
NC_000017.10:g.39739433G>A , CM000679.1:g.39739433G>A GRCh37
NC_000017.9:g.36992959G>A NCBI36
NG_008624.1:g.8715C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1275-41C>T MANE Select ENSP00000167586.6:n.1275-41C>T
ENST00000167586.6:c.1275-41C>T ENSP00000167586.6:n.1275-41C>T
ENST00000441550.2:n.222-41C>T
NM_000526.4:c.1275-41C>T NP_000517.2:n.1275-41C>T
NM_000526.5:c.1275-41C>T MANE Select NP_000517.3:n.1275-41C>T