Canonical Allele Identifier: CA2036520175
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488112A= , CM000674.2:g.52488112A= GRCh38
NC_000012.11:g.52881896A= , CM000674.1:g.52881896A= GRCh37
NC_000012.10:g.51168163A= NCBI36
NG_008298.1:g.10286T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1425-9T= MANE Select ENSP00000369317.3:n.1425-9T=
ENST00000330722.6:c.1425-9T= ENSP00000369317.3:n.1425-9T=
NM_005554.3:c.1425-9T= NP_005545.1:n.1425-9T=
NM_005554.4:c.1425-9T= MANE Select NP_005545.1:n.1425-9T=