Canonical Allele Identifier: CA8548017
Gene: KRT10 HGNC NCBI

Linked Data

dbSNP Id: rs771884630
ExAC: 17:38975308 GCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTT / G
gnomAD v2: 17-38975308-GCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTT-G
gnomAD v4: 17-40819056-GCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTT-G
MyVariant Identifiers: chr17:g.38975309_38975344del (hg19) chr17:g.38975315_38975386delinsCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTT (hg19) chr17:g.40819057_40819092del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819063_40819098del , CM000679.2:g.40819063_40819098del GRCh38
NC_000017.10:g.38975315_38975350del , CM000679.1:g.38975315_38975350del GRCh37
NC_000017.9:g.36228841_36228876del NCBI36
NG_008405.1:g.8520_8555del
NG_033147.1:g.4972_5007del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1443_1478del MANE Select ENSP00000269576.5:p.Ser482_Gly493del
ENST00000635956.2:c.1443_1478del ENSP00000490524.2:p.Ser482_Gly493del
ENST00000269576.5:c.1443_1478del ENSP00000269576.5:p.Ser482_Gly493del
NM_000421.3:c.1443_1478del NP_000412.3:p.Ser482_Gly493del
XM_005257343.2:c.1443_1478del XP_005257400.1:p.Ser482_Gly493del
XM_005257343.3:c.1443_1478del XP_005257400.1:p.Ser482_Gly493del
NM_000421.4:c.1443_1478del NP_000412.3:p.Ser482_Gly493del
NM_000421.5:c.1443_1478del MANE Select NP_000412.4:p.Ser482_Gly493del
NM_001379366.1:c.1443_1478del NP_001366295.1:p.Ser482_Gly493del
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