Canonical Allele Identifier: CA2036520247
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1938184887
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488242del , CM000674.2:g.52488242del GRCh38
NC_000012.11:g.52882026del , CM000674.1:g.52882026del GRCh37
NC_000012.10:g.51168293del NCBI36
NG_008298.1:g.10156del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1424+86del MANE Select ENSP00000369317.3:n.1424+86del
ENST00000330722.6:c.1424+86del ENSP00000369317.3:n.1424+86del
NM_005554.3:c.1424+86del NP_005545.1:n.1424+86del
NM_005554.4:c.1424+86del MANE Select NP_005545.1:n.1424+86del
Search 100 bp 5'
Search 100 bp 3'