Canonical Allele Identifier: CA626212573
Gene: KRT10 HGNC NCBI

Linked Data

dbSNP Id: rs1905212309
gnomAD v2: 17-38975317-GCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT-G
gnomAD v3: 17-40819065-GCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT-G
gnomAD v4: 17-40819065-GCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT-G
MyVariant Identifiers: chr17:g.38975318_38975398del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819074_40819154del , CM000679.2:g.40819074_40819154del GRCh38
NC_000017.10:g.38975326_38975406del , CM000679.1:g.38975326_38975406del GRCh37
NC_000017.9:g.36228852_36228932del NCBI36
NG_008405.1:g.8466_8546del
NG_033147.1:g.4983_5063del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1389_1469del MANE Select ENSP00000269576.5:p.Arg464_Gly490del
ENST00000635956.2:c.1389_1469del ENSP00000490524.2:p.Arg464_Gly490del
ENST00000269576.5:c.1389_1469del ENSP00000269576.5:p.Arg464_Gly490del
NM_000421.3:c.1389_1469del NP_000412.3:p.Arg464_Gly490del
XM_005257343.2:c.1389_1469del XP_005257400.1:p.Arg464_Gly490del
XM_005257343.3:c.1389_1469del XP_005257400.1:p.Arg464_Gly490del
NM_000421.4:c.1389_1469del NP_000412.3:p.Arg464_Gly490del
NM_000421.5:c.1389_1469del MANE Select NP_000412.4:p.Arg464_Gly490del
NM_001379366.1:c.1389_1469del NP_001366295.1:p.Arg464_Gly490del
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