Canonical Allele Identifier: CA2036520402
Gene: KRT6A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488519A= , CM000674.2:g.52488519A= GRCh38
NC_000012.11:g.52882303A= , CM000674.1:g.52882303A= GRCh37
NC_000012.10:g.51168570A= NCBI36
NG_008298.1:g.9879T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1233T= MANE Select ENSP00000369317.3:p.Asp411=
ENST00000330722.6:c.1233T= ENSP00000369317.3:p.Asp411=
NM_005554.3:c.1233T= NP_005545.1:p.Asp411=
NM_005554.4:c.1233T= MANE Select NP_005545.1:p.Asp411=
Search 100 bp 5'
Search 100 bp 3'