Canonical Allele Identifier: CA2542921033
Gene: KRT10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40818900_40819106del , CM000679.2:g.40818900_40819106del GRCh38
NC_000017.10:g.38975152_38975358del , CM000679.1:g.38975152_38975358del GRCh37
NC_000017.9:g.36228678_36228884del NCBI36
NG_008405.1:g.8520_8726del
NG_033147.1:g.4809_5015del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1443_1649del MANE Select ENSP00000269576.5:p.Ser482_Gly550del
ENST00000635956.2:c.1443_1649del ENSP00000490524.2:p.Ser482_Gly550del
ENST00000269576.5:c.1443_1649del ENSP00000269576.5:p.Ser482_Gly550del
NM_000421.3:c.1443_1649del NP_000412.3:p.Ser482_Gly550del
XM_005257343.2:c.1443_1649del XP_005257400.1:p.Ser482_Gly550del
XM_005257343.3:c.1443_1649del XP_005257400.1:p.Ser482_Gly550del
NM_000421.4:c.1443_1649del NP_000412.3:p.Ser482_Gly550del
NM_000421.5:c.1443_1649del MANE Select NP_000412.4:p.Ser482_Gly550del
NM_001379366.1:c.1443_1649del NP_001366295.1:p.Ser482_Gly550del
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