Canonical Allele Identifier: CA2036520070
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487929C= , CM000674.2:g.52487929C= GRCh38
NC_000012.11:g.52881713C= , CM000674.1:g.52881713C= GRCh37
NC_000012.10:g.51167980C= NCBI36
NG_008298.1:g.10469G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1486G= MANE Select ENSP00000369317.3:p.Gly496=
ENST00000330722.6:c.1486G= ENSP00000369317.3:p.Gly496=
NM_005554.3:c.1486G= NP_005545.1:p.Gly496=
NM_005554.4:c.1486G= MANE Select NP_005545.1:p.Gly496=