Canonical Allele Identifier: CA2576267701
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41584448-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584448C>A , CM000679.2:g.41584448C>A GRCh38
NC_000017.10:g.39740700C>A , CM000679.1:g.39740700C>A GRCh37
NC_000017.9:g.36994226C>A NCBI36
NG_008624.1:g.7448G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609-35G>T MANE Select ENSP00000167586.6:n.609-35G>T
ENST00000167586.6:c.609-35G>T ENSP00000167586.6:n.609-35G>T
ENST00000476662.1:n.24G>T
NM_000526.4:c.609-35G>T NP_000517.2:n.609-35G>T
NM_000526.5:c.609-35G>T MANE Select NP_000517.3:n.609-35G>T
Search 100 bp 5'
Search 100 bp 3'