Canonical Allele Identifier: CA2036520393
Gene: KRT6A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488503C= , CM000674.2:g.52488503C= GRCh38
NC_000012.11:g.52882287C= , CM000674.1:g.52882287C= GRCh37
NC_000012.10:g.51168554C= NCBI36
NG_008298.1:g.9895G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1249G= MANE Select ENSP00000369317.3:p.Glu417=
ENST00000330722.6:c.1249G= ENSP00000369317.3:p.Glu417=
NM_005554.3:c.1249G= NP_005545.1:p.Glu417=
NM_005554.4:c.1249G= MANE Select NP_005545.1:p.Glu417=
Search 100 bp 5'
Search 100 bp 3'