Canonical Allele Identifier: CA2036520167
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488095C= , CM000674.2:g.52488095C= GRCh38
NC_000012.11:g.52881879C= , CM000674.1:g.52881879C= GRCh37
NC_000012.10:g.51168146C= NCBI36
NG_008298.1:g.10303G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1433G= MANE Select ENSP00000369317.3:p.Gly478=
ENST00000330722.6:c.1433G= ENSP00000369317.3:p.Gly478=
NM_005554.3:c.1433G= NP_005545.1:p.Gly478=
NM_005554.4:c.1433G= MANE Select NP_005545.1:p.Gly478=