Canonical Allele Identifier: CA384963297
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492668A>T , CM000674.2:g.52492668A>T GRCh38
NC_000012.11:g.52886452A>T , CM000674.1:g.52886452A>T GRCh37
NC_000012.10:g.51172719A>T NCBI36
NG_008298.1:g.5730T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.521T>A MANE Select ENSP00000369317.3:p.Phe174Tyr
ENST00000330722.6:c.521T>A ENSP00000369317.3:p.Phe174Tyr
ENST00000549898.5:n.42T>A
NM_005554.3:c.521T>A NP_005545.1:p.Phe174Tyr
NM_005554.4:c.521T>A MANE Select NP_005545.1:p.Phe174Tyr