Canonical Allele Identifier: CA384963257
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492662G>C , CM000674.2:g.52492662G>C GRCh38
NC_000012.11:g.52886446G>C , CM000674.1:g.52886446G>C GRCh37
NC_000012.10:g.51172713G>C NCBI36
NG_008298.1:g.5736C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.527C>G MANE Select ENSP00000369317.3:p.Ser176Cys
ENST00000330722.6:c.527C>G ENSP00000369317.3:p.Ser176Cys
ENST00000549898.5:n.48C>G
NM_005554.3:c.527C>G NP_005545.1:p.Ser176Cys
NM_005554.4:c.527C>G MANE Select NP_005545.1:p.Ser176Cys