Canonical Allele Identifier: CA2259726771

Gene: KRT10 KRT10-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822238_40822268delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA , CM000679.2:g.40822238_40822268delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA	GRCh38
NC_000017.10:g.38978490_38978520delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA , CM000679.1:g.38978490_38978520delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA	GRCh37
NC_000017.9:g.36232016_36232046delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA	NCBI36
NG_008405.1:g.5344_5374delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC
NG_033147.1:g.8147_8177delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10) MANE Select	ENSP00000269576.5:p.Ser106=
ENST00000635956.2:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10)	ENSP00000490524.2:p.Ser106=
ENST00000269576.5:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10)	ENSP00000269576.5:p.Ser106=
ENST00000301665.7:c.-221+3030_-221+3060delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)	ENSP00000301665.3:n.-221+3030_-221+3060delinsGCTGCCCCCACCAAAG...
ENST00000436612.5:c.-221+3068_-221+3098delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)	ENSP00000390036.1:n.-221+3068_-221+3098delinsGCTGCCCCCACCAAAG...
ENST00000496847.1:n.49+3030_49+3060delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)
ENST00000622451.1:c.-221+2959_-221+2989delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)	ENSP00000482364.1:n.-221+2959_-221+2989delinsGCTGCCCCCACCAAAG...
NM_000421.3:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10)	NP_000412.3:p.Ser106=
NM_001195386.1:c.-221+2959_-221+2989delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)	NP_001182315.1:n.-221+2959_-221+2989delinsGCTGCCCCCACCAAAGCTG...
NM_001195387.1:c.-221+3068_-221+3098delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)	NP_001182316.1:n.-221+3068_-221+3098delinsGCTGCCCCCACCAAAGCTG...
NM_145274.3:c.-221+3030_-221+3060delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)	NP_660317.2:n.-221+3030_-221+3060delinsGCTGCCCCCACCAAAGCTGCCA...
XM_005257343.2:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10)	XP_005257400.1:p.Ser106=
XM_005257089.4:c.-461+3030_-461+3060delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)	XP_005257146.1:n.-461+3030_-461+3060delinsGCTGCCCCCACCAAAGCTG...
XM_005257343.3:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10)	XP_005257400.1:p.Ser106=
XM_017024253.1:c.-414+3030_-414+3060delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)	XP_016879742.1:n.-414+3030_-414+3060delinsGCTGCCCCCACCAAAGCTG...
NM_000421.4:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10)	NP_000412.3:p.Ser106=
NR_160886.1:n.95+2959_95+2989delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)
NR_160887.1:n.26+3068_26+3098delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)
NR_160888.1:n.64+3030_64+3060delinsGCTGCCCCCACCAAAGCTGCCACCTCCGAAA (KRT10-AS1)
NM_000421.5:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10) MANE Select	NP_000412.4:p.Ser106=
NM_001379366.1:c.318_348delinsTTTCGGAGGTGGCAGCTTTGGTGGGGGCAGC (KRT10)	NP_001366295.1:p.Ser106=