Canonical Allele Identifier: CA2618930452
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492571dup , CM000674.2:g.52492571dup GRCh38
NC_000012.11:g.52886355dup , CM000674.1:g.52886355dup GRCh37
NC_000012.10:g.51172622dup NCBI36
NG_008298.1:g.5828dup

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+79dup MANE Select ENSP00000369317.3:n.540+79dup
ENST00000330722.6:c.540+79dup ENSP00000369317.3:n.540+79dup
ENST00000549898.5:n.61+79dup
NM_005554.3:c.540+79dup NP_005545.1:n.540+79dup
NM_005554.4:c.540+79dup MANE Select NP_005545.1:n.540+79dup