Canonical Allele Identifier: CA983719558
Gene: KRT10 HGNC NCBI

Linked Data

dbSNP Id: rs1905180770

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40818895_40818996del , CM000679.2:g.40818895_40818996del GRCh38
NC_000017.10:g.38975147_38975248del , CM000679.1:g.38975147_38975248del GRCh37
NC_000017.9:g.36228673_36228774del NCBI36
NG_008405.1:g.8619_8720del
NG_033147.1:g.4804_4905del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1542_1643del MANE Select ENSP00000269576.5:p.Gly515_Gly548del
ENST00000635956.2:c.1542_1643del ENSP00000490524.2:p.Gly515_Gly548del
ENST00000269576.5:c.1542_1643del ENSP00000269576.5:p.Gly515_Gly548del
NM_000421.3:c.1542_1643del NP_000412.3:p.Gly515_Gly548del
XM_005257343.2:c.1542_1643del XP_005257400.1:p.Gly515_Gly548del
XM_005257343.3:c.1542_1643del XP_005257400.1:p.Gly515_Gly548del
NM_000421.4:c.1542_1643del NP_000412.3:p.Gly515_Gly548del
NM_000421.5:c.1542_1643del MANE Select NP_000412.4:p.Gly515_Gly548del
NM_001379366.1:c.1542_1643del NP_001366295.1:p.Gly515_Gly548del