Canonical Allele Identifier: CA2637768433
Gene: KRT10 HGNC NCBI

Linked Data

gnomAD v4: 17-40819055-TGCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819063_40819143del , CM000679.2:g.40819063_40819143del GRCh38
NC_000017.10:g.38975315_38975395del , CM000679.1:g.38975315_38975395del GRCh37
NC_000017.9:g.36228841_36228921del NCBI36
NG_008405.1:g.8476_8556del
NG_033147.1:g.4972_5052del

Transcript Alleles

HGVS Amino-acid change
ENST00000269576.6:c.1399_1479del MANE Select ENSP00000269576.5:p.Gly467_Gly493del
ENST00000635956.2:c.1399_1479del ENSP00000490524.2:p.Gly467_Gly493del
ENST00000269576.5:c.1399_1479del ENSP00000269576.5:p.Gly467_Gly493del
NM_000421.3:c.1399_1479del NP_000412.3:p.Gly467_Gly493del
XM_005257343.2:c.1399_1479del XP_005257400.1:p.Gly467_Gly493del
XM_005257343.3:c.1399_1479del XP_005257400.1:p.Gly467_Gly493del
NM_000421.4:c.1399_1479del NP_000412.3:p.Gly467_Gly493del
NM_000421.5:c.1399_1479del MANE Select NP_000412.4:p.Gly467_Gly493del
NM_001379366.1:c.1399_1479del NP_001366295.1:p.Gly467_Gly493del
Search 100 bp 5'
Search 100 bp 3'