Canonical Allele Identifier: CA2036520414
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488539G= , CM000674.2:g.52488539G= GRCh38
NC_000012.11:g.52882323G= , CM000674.1:g.52882323G= GRCh37
NC_000012.10:g.51168590G= NCBI36
NG_008298.1:g.9859C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1213C= MANE Select ENSP00000369317.3:p.Leu405=
ENST00000330722.6:c.1213C= ENSP00000369317.3:p.Leu405=
NM_005554.3:c.1213C= NP_005545.1:p.Leu405=
NM_005554.4:c.1213C= MANE Select NP_005545.1:p.Leu405=