Canonical Allele Identifier: CA2637771424
Gene: KRT10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40818956_40819006del , CM000679.2:g.40818956_40819006del GRCh38
NC_000017.10:g.38975208_38975258del , CM000679.1:g.38975208_38975258del GRCh37
NC_000017.9:g.36228734_36228784del NCBI36
NG_008405.1:g.8619_8669del
NG_033147.1:g.4865_4915del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1542_1592del MANE Select ENSP00000269576.5:p.Gly515_Gly531del
ENST00000635956.2:c.1542_1592del ENSP00000490524.2:p.Gly515_Gly531del
ENST00000269576.5:c.1542_1592del ENSP00000269576.5:p.Gly515_Gly531del
NM_000421.3:c.1542_1592del NP_000412.3:p.Gly515_Gly531del
XM_005257343.2:c.1542_1592del XP_005257400.1:p.Gly515_Gly531del
XM_005257343.3:c.1542_1592del XP_005257400.1:p.Gly515_Gly531del
NM_000421.4:c.1542_1592del NP_000412.3:p.Gly515_Gly531del
NM_000421.5:c.1542_1592del MANE Select NP_000412.4:p.Gly515_Gly531del
NM_001379366.1:c.1542_1592del NP_001366295.1:p.Gly515_Gly531del