Canonical Allele Identifier: CA2637768327
Gene: KRT10 HGNC NCBI

Linked Data

gnomAD v4: 17-40818993-CCCGTAGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCTCCGTAGCCGCCGCCGGAACTGCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819009_40819128del , CM000679.2:g.40819009_40819128del GRCh38
NC_000017.10:g.38975261_38975380del , CM000679.1:g.38975261_38975380del GRCh37
NC_000017.9:g.36228787_36228906del NCBI36
NG_008405.1:g.8499_8618del
NG_033147.1:g.4918_5037del

Transcript Alleles

HGVS Amino-acid change
ENST00000269576.6:c.1422_1541del MANE Select ENSP00000269576.5:p.Gly475_Gly514del
ENST00000635956.2:c.1422_1541del ENSP00000490524.2:p.Gly475_Gly514del
ENST00000269576.5:c.1422_1541del ENSP00000269576.5:p.Gly475_Gly514del
NM_000421.3:c.1422_1541del NP_000412.3:p.Gly475_Gly514del
XM_005257343.2:c.1422_1541del XP_005257400.1:p.Gly475_Gly514del
XM_005257343.3:c.1422_1541del XP_005257400.1:p.Gly475_Gly514del
NM_000421.4:c.1422_1541del NP_000412.3:p.Gly475_Gly514del
NM_000421.5:c.1422_1541del MANE Select NP_000412.4:p.Gly475_Gly514del
NM_001379366.1:c.1422_1541del NP_001366295.1:p.Gly475_Gly514del
Search 100 bp 5'
Search 100 bp 3'