Canonical Allele Identifier: CA500186326
Gene: KRT10 HGNC NCBI
KRT10-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40822538_40822540dup , CM000679.2:g.40822538_40822540dup GRCh38
NC_000017.10:g.38978790_38978792dup , CM000679.1:g.38978790_38978792dup GRCh37
NC_000017.9:g.36232316_36232318dup NCBI36
NG_008405.1:g.5072_5074dup
NG_033147.1:g.8447_8449dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.46_48dup (KRT10) MANE Select ENSP00000269576.5:p.Ser16_Gly17insSer
ENST00000635956.2:c.46_48dup (KRT10) ENSP00000490524.2:p.Ser16_Gly17insSer
ENST00000269576.5:c.46_48dup (KRT10) ENSP00000269576.5:p.Ser16_Gly17insSer
ENST00000301665.7:c.-221+3330_-221+3332dup (KRT10-AS1) ENSP00000301665.3:n.-221+3330_-221+3332dup
ENST00000436612.5:c.-221+3368_-221+3370dup (KRT10-AS1) ENSP00000390036.1:n.-221+3368_-221+3370dup
ENST00000496847.1:n.49+3330_49+3332dup (KRT10-AS1)
ENST00000622451.1:c.-221+3259_-221+3261dup (KRT10-AS1) ENSP00000482364.1:n.-221+3259_-221+3261dup
NM_000421.3:c.46_48dup (KRT10) NP_000412.3:p.Ser16_Gly17insSer
NM_001195386.1:c.-221+3259_-221+3261dup (KRT10-AS1) NP_001182315.1:n.-221+3259_-221+3261dup
NM_001195387.1:c.-221+3368_-221+3370dup (KRT10-AS1) NP_001182316.1:n.-221+3368_-221+3370dup
NM_145274.3:c.-221+3330_-221+3332dup (KRT10-AS1) NP_660317.2:n.-221+3330_-221+3332dup
XM_005257343.2:c.46_48dup (KRT10) XP_005257400.1:p.Ser16_Gly17insSer
XM_005257089.4:c.-461+3330_-461+3332dup (KRT10-AS1) XP_005257146.1:n.-461+3330_-461+3332dup
XM_005257343.3:c.46_48dup (KRT10) XP_005257400.1:p.Ser16_Gly17insSer
XM_017024253.1:c.-414+3330_-414+3332dup (KRT10-AS1) XP_016879742.1:n.-414+3330_-414+3332dup
NM_000421.4:c.46_48dup (KRT10) NP_000412.3:p.Ser16_Gly17insSer
NR_160886.1:n.95+3259_95+3261dup (KRT10-AS1)
NR_160887.1:n.26+3368_26+3370dup (KRT10-AS1)
NR_160888.1:n.64+3330_64+3332dup (KRT10-AS1)
NM_000421.5:c.46_48dup (KRT10) MANE Select NP_000412.4:p.Ser16_Gly17insSer
NM_001379366.1:c.46_48dup (KRT10) NP_001366295.1:p.Ser16_Gly17insSer