Canonical Allele Identifier: CA605240666
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1418120513

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488277del , CM000674.2:g.52488277del GRCh38
NC_000012.11:g.52882061del , CM000674.1:g.52882061del GRCh37
NC_000012.10:g.51168328del NCBI36
NG_008298.1:g.10122del

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.1424+52del MANE Select ENSP00000369317.3:n.1424+52del
ENST00000330722.6:c.1424+52del ENSP00000369317.3:n.1424+52del
NM_005554.3:c.1424+52del NP_005545.1:n.1424+52del
NM_005554.4:c.1424+52del MANE Select NP_005545.1:n.1424+52del