Canonical Allele Identifier: CA2542921539
Gene: KRT10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40818882_40819028del , CM000679.2:g.40818882_40819028del GRCh38
NC_000017.10:g.38975134_38975280del , CM000679.1:g.38975134_38975280del GRCh37
NC_000017.9:g.36228660_36228806del NCBI36
NG_008405.1:g.8599_8745del
NG_033147.1:g.4791_4937del

Transcript Alleles

HGVS Amino-acid change
ENST00000269576.6:c.1522_1668del MANE Select ENSP00000269576.5:p.Ser508_Gly556del
ENST00000635956.2:c.1522_1668del ENSP00000490524.2:p.Ser508_Gly556del
ENST00000269576.5:c.1522_1668del ENSP00000269576.5:p.Ser508_Gly556del
NM_000421.3:c.1522_1668del NP_000412.3:p.Ser508_Gly556del
XM_005257343.2:c.1522_1668del XP_005257400.1:p.Ser508_Gly556del
XM_005257343.3:c.1522_1668del XP_005257400.1:p.Ser508_Gly556del
NM_000421.4:c.1522_1668del NP_000412.3:p.Ser508_Gly556del
NM_000421.5:c.1522_1668del MANE Select NP_000412.4:p.Ser508_Gly556del
NM_001379366.1:c.1522_1668del NP_001366295.1:p.Ser508_Gly556del
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