Canonical Allele Identifier: CA2036520269
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488278A= , CM000674.2:g.52488278A= GRCh38
NC_000012.11:g.52882062A= , CM000674.1:g.52882062A= GRCh37
NC_000012.10:g.51168329A= NCBI36
NG_008298.1:g.10120T=

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.1424+50T= MANE Select ENSP00000369317.3:n.1424+50T=
ENST00000330722.6:c.1424+50T= ENSP00000369317.3:n.1424+50T=
NM_005554.3:c.1424+50T= NP_005545.1:n.1424+50T=
NM_005554.4:c.1424+50T= MANE Select NP_005545.1:n.1424+50T=