Canonical Allele Identifier: CA983719808
Gene: KRT10 HGNC NCBI

Linked Data

gnomAD v3: 17-40818911-AGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCGCCGCCGGAGCT-A
gnomAD v4: 17-40818911-AGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCGCCGCCGGAGCT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40818912_40819013del , CM000679.2:g.40818912_40819013del GRCh38
NC_000017.10:g.38975164_38975265del , CM000679.1:g.38975164_38975265del GRCh37
NC_000017.9:g.36228690_36228791del NCBI36
NG_008405.1:g.8599_8700del
NG_033147.1:g.4821_4922del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1522_1623del MANE Select ENSP00000269576.5:p.Ser508_Gly541del
ENST00000635956.2:c.1522_1623del ENSP00000490524.2:p.Ser508_Gly541del
ENST00000269576.5:c.1522_1623del ENSP00000269576.5:p.Ser508_Gly541del
NM_000421.3:c.1522_1623del NP_000412.3:p.Ser508_Gly541del
XM_005257343.2:c.1522_1623del XP_005257400.1:p.Ser508_Gly541del
XM_005257343.3:c.1522_1623del XP_005257400.1:p.Ser508_Gly541del
NM_000421.4:c.1522_1623del NP_000412.3:p.Ser508_Gly541del
NM_000421.5:c.1522_1623del MANE Select NP_000412.4:p.Ser508_Gly541del
NM_001379366.1:c.1522_1623del NP_001366295.1:p.Ser508_Gly541del
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