Canonical Allele Identifier: CA384952649
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487856C>A , CM000674.2:g.52487856C>A GRCh38
NC_000012.11:g.52881640C>A , CM000674.1:g.52881640C>A GRCh37
NC_000012.10:g.51167907C>A NCBI36
NG_008298.1:g.10542G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1559G>T MANE Select ENSP00000369317.3:p.Gly520Val
ENST00000330722.6:c.1559G>T ENSP00000369317.3:p.Gly520Val
NM_005554.3:c.1559G>T NP_005545.1:p.Gly520Val
NM_005554.4:c.1559G>T MANE Select NP_005545.1:p.Gly520Val