Canonical Allele Identifier: CA2036520072
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487932T= , CM000674.2:g.52487932T= GRCh38
NC_000012.11:g.52881716T= , CM000674.1:g.52881716T= GRCh37
NC_000012.10:g.51167983T= NCBI36
NG_008298.1:g.10466A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1483A= MANE Select ENSP00000369317.3:p.Ser495=
ENST00000330722.6:c.1483A= ENSP00000369317.3:p.Ser495=
NM_005554.3:c.1483A= NP_005545.1:p.Ser495=
NM_005554.4:c.1483A= MANE Select NP_005545.1:p.Ser495=