Canonical Allele Identifier: CA983718941
Gene: KRT10 HGNC NCBI

Linked Data

gnomAD v3: 17-40818843-TCCGCTGGAGCTGCCGCCGCCGTATCCGCCGCCGGAGCTGCTGCCGCCGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCG-T
gnomAD v4: 17-40818843-TCCGCTGGAGCTGCCGCCGCCGTATCCGCCGCCGGAGCTGCTGCCGCCGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40818848_40819006del , CM000679.2:g.40818848_40819006del GRCh38
NC_000017.10:g.38975100_38975258del , CM000679.1:g.38975100_38975258del GRCh37
NC_000017.9:g.36228626_36228784del NCBI36
NG_008405.1:g.8610_8768del
NG_033147.1:g.4757_4915del

Transcript Alleles

HGVS Amino-acid change
ENST00000269576.6:c.1533_1691del MANE Select ENSP00000269576.5:p.Gly512_Gly564del
ENST00000635956.2:c.1533_1691del ENSP00000490524.2:p.Gly512_Gly564del
ENST00000269576.5:c.1533_1691del ENSP00000269576.5:p.Gly512_Gly564del
NM_000421.3:c.1533_1691del NP_000412.3:p.Gly512_Gly564del
XM_005257343.2:c.1533_1691del XP_005257400.1:p.Gly512_Gly564del
XM_005257343.3:c.1533_1691del XP_005257400.1:p.Gly512_Gly564del
NM_000421.4:c.1533_1691del NP_000412.3:p.Gly512_Gly564del
NM_000421.5:c.1533_1691del MANE Select NP_000412.4:p.Gly512_Gly564del
NM_001379366.1:c.1533_1691del NP_001366295.1:p.Gly512_Gly564del
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