Canonical Allele Identifier: CA2036520296
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488325C= , CM000674.2:g.52488325C= GRCh38
NC_000012.11:g.52882109C= , CM000674.1:g.52882109C= GRCh37
NC_000012.10:g.51168376C= NCBI36
NG_008298.1:g.10073G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1424+3G= MANE Select ENSP00000369317.3:n.1424+3G=
ENST00000330722.6:c.1424+3G= ENSP00000369317.3:n.1424+3G=
NM_005554.3:c.1424+3G= NP_005545.1:n.1424+3G=
NM_005554.4:c.1424+3G= MANE Select NP_005545.1:n.1424+3G=