Canonical Allele Identifier: CA2036520417
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488545C= , CM000674.2:g.52488545C= GRCh38
NC_000012.11:g.52882329C= , CM000674.1:g.52882329C= GRCh37
NC_000012.10:g.51168596C= NCBI36
NG_008298.1:g.9853G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1207G= MANE Select ENSP00000369317.3:p.Ala403=
ENST00000330722.6:c.1207G= ENSP00000369317.3:p.Ala403=
NM_005554.3:c.1207G= NP_005545.1:p.Ala403=
NM_005554.4:c.1207G= MANE Select NP_005545.1:p.Ala403=