Canonical Allele Identifier: CA384954788
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488536G>T , CM000674.2:g.52488536G>T GRCh38
NC_000012.11:g.52882320G>T , CM000674.1:g.52882320G>T GRCh37
NC_000012.10:g.51168587G>T NCBI36
NG_008298.1:g.9862C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1216C>A MANE Select ENSP00000369317.3:p.Gln406Lys
ENST00000330722.6:c.1216C>A ENSP00000369317.3:p.Gln406Lys
NM_005554.3:c.1216C>A NP_005545.1:p.Gln406Lys
NM_005554.4:c.1216C>A MANE Select NP_005545.1:p.Gln406Lys