Canonical Allele Identifier: CA2036520300
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488332A= , CM000674.2:g.52488332A= GRCh38
NC_000012.11:g.52882116A= , CM000674.1:g.52882116A= GRCh37
NC_000012.10:g.51168383A= NCBI36
NG_008298.1:g.10066T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1420T= MANE Select ENSP00000369317.3:p.Cys474=
ENST00000330722.6:c.1420T= ENSP00000369317.3:p.Cys474=
NM_005554.3:c.1420T= NP_005545.1:p.Cys474=
NM_005554.4:c.1420T= MANE Select NP_005545.1:p.Cys474=