Canonical Allele Identifier: CA2637768343
Gene: KRT10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819024_40819143del , CM000679.2:g.40819024_40819143del GRCh38
NC_000017.10:g.38975276_38975395del , CM000679.1:g.38975276_38975395del GRCh37
NC_000017.9:g.36228802_36228921del NCBI36
NG_008405.1:g.8481_8600del
NG_033147.1:g.4933_5052del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1404_1523del MANE Select ENSP00000269576.5:p.Phe469_Ser508del
ENST00000635956.2:c.1404_1523del ENSP00000490524.2:p.Phe469_Ser508del
ENST00000269576.5:c.1404_1523del ENSP00000269576.5:p.Phe469_Ser508del
NM_000421.3:c.1404_1523del NP_000412.3:p.Phe469_Ser508del
XM_005257343.2:c.1404_1523del XP_005257400.1:p.Phe469_Ser508del
XM_005257343.3:c.1404_1523del XP_005257400.1:p.Phe469_Ser508del
NM_000421.4:c.1404_1523del NP_000412.3:p.Phe469_Ser508del
NM_000421.5:c.1404_1523del MANE Select NP_000412.4:p.Phe469_Ser508del
NM_001379366.1:c.1404_1523del NP_001366295.1:p.Phe469_Ser508del