Canonical Allele Identifier: CA2637768348
Gene: KRT10 HGNC NCBI

Linked Data

gnomAD v4: 17-40819014-TCCGCCGCCGGAGCTTCCGCCTCCGTAGCCGCCGCCGGAACTGCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819024_40819128del , CM000679.2:g.40819024_40819128del GRCh38
NC_000017.10:g.38975276_38975380del , CM000679.1:g.38975276_38975380del GRCh37
NC_000017.9:g.36228802_36228906del NCBI36
NG_008405.1:g.8493_8597del
NG_033147.1:g.4933_5037del

Transcript Alleles

HGVS Amino-acid change
ENST00000269576.6:c.1416_1520del MANE Select ENSP00000269576.5:p.Tyr473_Gly507del
ENST00000635956.2:c.1416_1520del ENSP00000490524.2:p.Tyr473_Gly507del
ENST00000269576.5:c.1416_1520del ENSP00000269576.5:p.Tyr473_Gly507del
NM_000421.3:c.1416_1520del NP_000412.3:p.Tyr473_Gly507del
XM_005257343.2:c.1416_1520del XP_005257400.1:p.Tyr473_Gly507del
XM_005257343.3:c.1416_1520del XP_005257400.1:p.Tyr473_Gly507del
NM_000421.4:c.1416_1520del NP_000412.3:p.Tyr473_Gly507del
NM_000421.5:c.1416_1520del MANE Select NP_000412.4:p.Tyr473_Gly507del
NM_001379366.1:c.1416_1520del NP_001366295.1:p.Tyr473_Gly507del
Search 100 bp 5'
Search 100 bp 3'