Canonical Allele Identifier: CA2637771430
Gene: KRT10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40818980_40819084del , CM000679.2:g.40818980_40819084del GRCh38
NC_000017.10:g.38975232_38975336del , CM000679.1:g.38975232_38975336del GRCh37
NC_000017.9:g.36228758_36228862del NCBI36
NG_008405.1:g.8545_8649del
NG_033147.1:g.4889_4993del

Transcript Alleles

HGVS Amino-acid change
ENST00000269576.6:c.1468_1572del MANE Select ENSP00000269576.5:p.Gly490_Gly524del
ENST00000635956.2:c.1468_1572del ENSP00000490524.2:p.Gly490_Gly524del
ENST00000269576.5:c.1468_1572del ENSP00000269576.5:p.Gly490_Gly524del
NM_000421.3:c.1468_1572del NP_000412.3:p.Gly490_Gly524del
XM_005257343.2:c.1468_1572del XP_005257400.1:p.Gly490_Gly524del
XM_005257343.3:c.1468_1572del XP_005257400.1:p.Gly490_Gly524del
NM_000421.4:c.1468_1572del NP_000412.3:p.Gly490_Gly524del
NM_000421.5:c.1468_1572del MANE Select NP_000412.4:p.Gly490_Gly524del
NM_001379366.1:c.1468_1572del NP_001366295.1:p.Gly490_Gly524del