Canonical Allele Identifier: CA2259726895

Gene: KRT10 KRT10-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822494_40822521delinsACTCCTCCTCCTCCTCCACATCCTCCTC , CM000679.2:g.40822494_40822521delinsACTCCTCCTCCTCCTCCACATCCTCCTC	GRCh38
NC_000017.10:g.38978746_38978773delinsACTCCTCCTCCTCCTCCACATCCTCCTC , CM000679.1:g.38978746_38978773delinsACTCCTCCTCCTCCTCCACATCCTCCTC	GRCh37
NC_000017.9:g.36232272_36232299delinsACTCCTCCTCCTCCTCCACATCCTCCTC	NCBI36
NG_008405.1:g.5091_5118delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT
NG_033147.1:g.8403_8430delinsACTCCTCCTCCTCCTCCACATCCTCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10) MANE Select	ENSP00000269576.5:p.Gly22=
ENST00000635956.2:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10)	ENSP00000490524.2:p.Gly22=
ENST00000269576.5:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10)	ENSP00000269576.5:p.Gly22=
ENST00000301665.7:c.-221+3286_-221+3313delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)	ENSP00000301665.3:n.-221+3286_-221+3313delinsACTCCTCCTCCTCCTC...
ENST00000436612.5:c.-221+3324_-221+3351delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)	ENSP00000390036.1:n.-221+3324_-221+3351delinsACTCCTCCTCCTCCTC...
ENST00000496847.1:n.49+3286_49+3313delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)
ENST00000622451.1:c.-221+3215_-221+3242delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)	ENSP00000482364.1:n.-221+3215_-221+3242delinsACTCCTCCTCCTCCTC...
NM_000421.3:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10)	NP_000412.3:p.Gly22=
NM_001195386.1:c.-221+3215_-221+3242delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)	NP_001182315.1:n.-221+3215_-221+3242delinsACTCCTCCTCCTCCTCCAC...
NM_001195387.1:c.-221+3324_-221+3351delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)	NP_001182316.1:n.-221+3324_-221+3351delinsACTCCTCCTCCTCCTCCAC...
NM_145274.3:c.-221+3286_-221+3313delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)	NP_660317.2:n.-221+3286_-221+3313delinsACTCCTCCTCCTCCTCCACATC...
XM_005257343.2:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10)	XP_005257400.1:p.Gly22=
XM_005257089.4:c.-461+3286_-461+3313delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)	XP_005257146.1:n.-461+3286_-461+3313delinsACTCCTCCTCCTCCTCCAC...
XM_005257343.3:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10)	XP_005257400.1:p.Gly22=
XM_017024253.1:c.-414+3286_-414+3313delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)	XP_016879742.1:n.-414+3286_-414+3313delinsACTCCTCCTCCTCCTCCAC...
NM_000421.4:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10)	NP_000412.3:p.Gly22=
NR_160886.1:n.95+3215_95+3242delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)
NR_160887.1:n.26+3324_26+3351delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)
NR_160888.1:n.64+3286_64+3313delinsACTCCTCCTCCTCCTCCACATCCTCCTC (KRT10-AS1)
NM_000421.5:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10) MANE Select	NP_000412.4:p.Gly22=
NM_001379366.1:c.65_92delinsGAGGAGGATGTGGAGGAGGAGGAGGAGT (KRT10)	NP_001366295.1:p.Gly22=