Canonical Allele Identifier: CA2036520076
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1938177520
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487941_52487943del , CM000674.2:g.52487941_52487943del GRCh38
NC_000012.11:g.52881725_52881727del , CM000674.1:g.52881725_52881727del GRCh37
NC_000012.10:g.51167992_51167994del NCBI36
NG_008298.1:g.10457_10459del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1474_1476del MANE Select ENSP00000369317.3:p.Thr492del
ENST00000330722.6:c.1474_1476del ENSP00000369317.3:p.Thr492del
NM_005554.3:c.1474_1476del NP_005545.1:p.Thr492del
NM_005554.4:c.1474_1476del MANE Select NP_005545.1:p.Thr492del
Search 100 bp 5'
Search 100 bp 3'