Canonical Allele Identifier: CA2036520193
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488145C= , CM000674.2:g.52488145C= GRCh38
NC_000012.11:g.52881929C= , CM000674.1:g.52881929C= GRCh37
NC_000012.10:g.51168196C= NCBI36
NG_008298.1:g.10253G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1425-42G= MANE Select ENSP00000369317.3:n.1425-42G=
ENST00000330722.6:c.1425-42G= ENSP00000369317.3:n.1425-42G=
NM_005554.3:c.1425-42G= NP_005545.1:n.1425-42G=
NM_005554.4:c.1425-42G= MANE Select NP_005545.1:n.1425-42G=