Canonical Allele Identifier: CA384952869
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487919C>A , CM000674.2:g.52487919C>A GRCh38
NC_000012.11:g.52881703C>A , CM000674.1:g.52881703C>A GRCh37
NC_000012.10:g.51167970C>A NCBI36
NG_008298.1:g.10479G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1496G>T MANE Select ENSP00000369317.3:p.Gly499Val
ENST00000330722.6:c.1496G>T ENSP00000369317.3:p.Gly499Val
NM_005554.3:c.1496G>T NP_005545.1:p.Gly499Val
NM_005554.4:c.1496G>T MANE Select NP_005545.1:p.Gly499Val