Canonical Allele Identifier: CA2036520407
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488528G= , CM000674.2:g.52488528G= GRCh38
NC_000012.11:g.52882312G= , CM000674.1:g.52882312G= GRCh37
NC_000012.10:g.51168579G= NCBI36
NG_008298.1:g.9870C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1224C= MANE Select ENSP00000369317.3:p.Ala408=
ENST00000330722.6:c.1224C= ENSP00000369317.3:p.Ala408=
NM_005554.3:c.1224C= NP_005545.1:p.Ala408=
NM_005554.4:c.1224C= MANE Select NP_005545.1:p.Ala408=