Canonical Allele Identifier: CA2564719496
Gene: KRT14 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583715A>G , CM000679.2:g.41583715A>G GRCh38
NC_000017.10:g.39739967A>G , CM000679.1:g.39739967A>G GRCh37
NC_000017.9:g.36993493A>G NCBI36
NG_008624.1:g.8181T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.928-39T>C MANE Select ENSP00000167586.6:n.928-39T>C
ENST00000167586.6:c.928-39T>C ENSP00000167586.6:n.928-39T>C
ENST00000476662.1:n.378-39T>C
NM_000526.4:c.928-39T>C NP_000517.2:n.928-39T>C
NM_000526.5:c.928-39T>C MANE Select NP_000517.3:n.928-39T>C
Search 100 bp 5'
Search 100 bp 3'