Canonical Allele Identifier: CA384963539
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492695T>C , CM000674.2:g.52492695T>C GRCh38
NC_000012.11:g.52886479T>C , CM000674.1:g.52886479T>C GRCh37
NC_000012.10:g.51172746T>C NCBI36
NG_008298.1:g.5703A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.494A>G MANE Select ENSP00000369317.3:p.Glu165Gly
ENST00000330722.6:c.494A>G ENSP00000369317.3:p.Glu165Gly
ENST00000549898.5:n.15A>G
NM_005554.3:c.494A>G NP_005545.1:p.Glu165Gly
NM_005554.4:c.494A>G MANE Select NP_005545.1:p.Glu165Gly