Canonical Allele Identifier: CA2036520216
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488180G= , CM000674.2:g.52488180G= GRCh38
NC_000012.11:g.52881964G= , CM000674.1:g.52881964G= GRCh37
NC_000012.10:g.51168231G= NCBI36
NG_008298.1:g.10218C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1425-77C= MANE Select ENSP00000369317.3:n.1425-77C=
ENST00000330722.6:c.1425-77C= ENSP00000369317.3:n.1425-77C=
NM_005554.3:c.1425-77C= NP_005545.1:n.1425-77C=
NM_005554.4:c.1425-77C= MANE Select NP_005545.1:n.1425-77C=