Canonical Allele Identifier: CA2036522738
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492679G= , CM000674.2:g.52492679G= GRCh38
NC_000012.11:g.52886463G= , CM000674.1:g.52886463G= GRCh37
NC_000012.10:g.51172730G= NCBI36
NG_008298.1:g.5719C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.510C= MANE Select ENSP00000369317.3:p.Leu170=
ENST00000330722.6:c.510C= ENSP00000369317.3:p.Leu170=
ENST00000549898.5:n.31C=
NM_005554.3:c.510C= NP_005545.1:p.Leu170=
NM_005554.4:c.510C= MANE Select NP_005545.1:p.Leu170=