Canonical Allele Identifier: CA499992002
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39742721G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586469G>A , CM000679.2:g.41586469G>A GRCh38
NC_000017.10:g.39742721G>A , CM000679.1:g.39742721G>A GRCh37
NC_000017.9:g.36996247G>A NCBI36
NG_008624.1:g.5427C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.366C>T MANE Select ENSP00000167586.6:p.Leu122=
ENST00000167586.6:c.366C>T ENSP00000167586.6:p.Leu122=
NM_000526.4:c.366C>T NP_000517.2:p.Leu122=
NM_000526.5:c.366C>T MANE Select NP_000517.3:p.Leu122=