Canonical Allele Identifier: CA6581910
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs778326332

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488527T>A , CM000674.2:g.52488527T>A GRCh38
NC_000012.11:g.52882311T>A , CM000674.1:g.52882311T>A GRCh37
NC_000012.10:g.51168578T>A NCBI36
NG_008298.1:g.9871A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1225A>T MANE Select ENSP00000369317.3:p.Ile409Phe
ENST00000330722.6:c.1225A>T ENSP00000369317.3:p.Ile409Phe
NM_005554.3:c.1225A>T NP_005545.1:p.Ile409Phe
NM_005554.4:c.1225A>T MANE Select NP_005545.1:p.Ile409Phe