Canonical Allele Identifier: CA2036520068
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487925T= , CM000674.2:g.52487925T= GRCh38
NC_000012.11:g.52881709T= , CM000674.1:g.52881709T= GRCh37
NC_000012.10:g.51167976T= NCBI36
NG_008298.1:g.10473A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1490A= MANE Select ENSP00000369317.3:p.Tyr497=
ENST00000330722.6:c.1490A= ENSP00000369317.3:p.Tyr497=
NM_005554.3:c.1490A= NP_005545.1:p.Tyr497=
NM_005554.4:c.1490A= MANE Select NP_005545.1:p.Tyr497=