Canonical Allele Identifier: CA384963255
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492662G>A , CM000674.2:g.52492662G>A GRCh38
NC_000012.11:g.52886446G>A , CM000674.1:g.52886446G>A GRCh37
NC_000012.10:g.51172713G>A NCBI36
NG_008298.1:g.5736C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.527C>T MANE Select ENSP00000369317.3:p.Ser176Phe
ENST00000330722.6:c.527C>T ENSP00000369317.3:p.Ser176Phe
ENST00000549898.5:n.48C>T
NM_005554.3:c.527C>T NP_005545.1:p.Ser176Phe
NM_005554.4:c.527C>T MANE Select NP_005545.1:p.Ser176Phe