Canonical Allele Identifier: CA2036520071
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487931C= , CM000674.2:g.52487931C= GRCh38
NC_000012.11:g.52881715C= , CM000674.1:g.52881715C= GRCh37
NC_000012.10:g.51167982C= NCBI36
NG_008298.1:g.10467G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1484G= MANE Select ENSP00000369317.3:p.Ser495=
ENST00000330722.6:c.1484G= ENSP00000369317.3:p.Ser495=
NM_005554.3:c.1484G= NP_005545.1:p.Ser495=
NM_005554.4:c.1484G= MANE Select NP_005545.1:p.Ser495=