Canonical Allele Identifier: CA384952980
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487935A>T , CM000674.2:g.52487935A>T GRCh38
NC_000012.11:g.52881719A>T , CM000674.1:g.52881719A>T GRCh37
NC_000012.10:g.51167986A>T NCBI36
NG_008298.1:g.10463T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1480T>A MANE Select ENSP00000369317.3:p.Ser494Thr
ENST00000330722.6:c.1480T>A ENSP00000369317.3:p.Ser494Thr
NM_005554.3:c.1480T>A NP_005545.1:p.Ser494Thr
NM_005554.4:c.1480T>A MANE Select NP_005545.1:p.Ser494Thr