Canonical Allele Identifier: CA2260085432
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583507C= , CM000679.2:g.41583507C= GRCh38
NC_000017.10:g.39739759C= , CM000679.1:g.39739759C= GRCh37
NC_000017.9:g.36993285C= NCBI36
NG_008624.1:g.8389G=

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1053+44G= MANE Select ENSP00000167586.6:n.1053+44G=
ENST00000167586.6:c.1053+44G= ENSP00000167586.6:n.1053+44G=
ENST00000476662.1:n.503+44G=
NM_000526.4:c.1053+44G= NP_000517.2:n.1053+44G=
NM_000526.5:c.1053+44G= MANE Select NP_000517.3:n.1053+44G=
Search 100 bp 5'
Search 100 bp 3'