Canonical Allele Identifier: CA2036520054
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487901C= , CM000674.2:g.52487901C= GRCh38
NC_000012.11:g.52881685C= , CM000674.1:g.52881685C= GRCh37
NC_000012.10:g.51167952C= NCBI36
NG_008298.1:g.10497G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1514G= MANE Select ENSP00000369317.3:p.Ser505=
ENST00000330722.6:c.1514G= ENSP00000369317.3:p.Ser505=
NM_005554.3:c.1514G= NP_005545.1:p.Ser505=
NM_005554.4:c.1514G= MANE Select NP_005545.1:p.Ser505=