Canonical Allele Identifier: CA2576267614
Gene: KRT14 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583685A>C , CM000679.2:g.41583685A>C GRCh38
NC_000017.10:g.39739937A>C , CM000679.1:g.39739937A>C GRCh37
NC_000017.9:g.36993463A>C NCBI36
NG_008624.1:g.8211T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.928-9T>G MANE Select ENSP00000167586.6:n.928-9T>G
ENST00000167586.6:c.928-9T>G ENSP00000167586.6:n.928-9T>G
ENST00000476662.1:n.378-9T>G
NM_000526.4:c.928-9T>G NP_000517.2:n.928-9T>G
NM_000526.5:c.928-9T>G MANE Select NP_000517.3:n.928-9T>G