Canonical Allele Identifier: CA2036522687
Gene: KRT6A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492588G= , CM000674.2:g.52492588G= GRCh38
NC_000012.11:g.52886372G= , CM000674.1:g.52886372G= GRCh37
NC_000012.10:g.51172639G= NCBI36
NG_008298.1:g.5810C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.540+61C= MANE Select ENSP00000369317.3:n.540+61C=
ENST00000330722.6:c.540+61C= ENSP00000369317.3:n.540+61C=
ENST00000549898.5:n.61+61C=
NM_005554.3:c.540+61C= NP_005545.1:n.540+61C=
NM_005554.4:c.540+61C= MANE Select NP_005545.1:n.540+61C=
Search 100 bp 5'
Search 100 bp 3'