Canonical Allele Identifier: CA2036520321
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488367A= , CM000674.2:g.52488367A= GRCh38
NC_000012.11:g.52882151A= , CM000674.1:g.52882151A= GRCh37
NC_000012.10:g.51168418A= NCBI36
NG_008298.1:g.10031T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1385T= MANE Select ENSP00000369317.3:p.Ile462=
ENST00000330722.6:c.1385T= ENSP00000369317.3:p.Ile462=
NM_005554.3:c.1385T= NP_005545.1:p.Ile462=
NM_005554.4:c.1385T= MANE Select NP_005545.1:p.Ile462=