Canonical Allele Identifier: CA2809476187

Gene: KRT10 KRT10-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822227_40822228insA , CM000679.2:g.40822227_40822228insA	GRCh38
NC_000017.10:g.38978479_38978480insA , CM000679.1:g.38978479_38978480insA	GRCh37
NC_000017.9:g.36232005_36232006insA	NCBI36
NG_008405.1:g.5384_5385insT
NG_033147.1:g.8136_8137insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.358_359insT (KRT10) MANE Select	ENSP00000269576.5:p.Gly120ValfsTer27
ENST00000635956.2:c.358_359insT (KRT10)	ENSP00000490524.2:p.Gly120ValfsTer27
ENST00000269576.5:c.358_359insT (KRT10)	ENSP00000269576.5:p.Gly120ValfsTer27
ENST00000301665.7:c.-221+3019_-221+3020insA (KRT10-AS1)	ENSP00000301665.3:n.-221+3019_-221+3020insA
ENST00000436612.5:c.-221+3057_-221+3058insA (KRT10-AS1)	ENSP00000390036.1:n.-221+3057_-221+3058insA
ENST00000496847.1:n.49+3019_49+3020insA (KRT10-AS1)
ENST00000622451.1:c.-221+2948_-221+2949insA (KRT10-AS1)	ENSP00000482364.1:n.-221+2948_-221+2949insA
NM_000421.3:c.358_359insT (KRT10)	NP_000412.3:p.Gly120ValfsTer27
NM_001195386.1:c.-221+2948_-221+2949insA (KRT10-AS1)	NP_001182315.1:n.-221+2948_-221+2949insA
NM_001195387.1:c.-221+3057_-221+3058insA (KRT10-AS1)	NP_001182316.1:n.-221+3057_-221+3058insA
NM_145274.3:c.-221+3019_-221+3020insA (KRT10-AS1)	NP_660317.2:n.-221+3019_-221+3020insA
XM_005257343.2:c.358_359insT (KRT10)	XP_005257400.1:p.Gly120ValfsTer27
XM_005257089.4:c.-461+3019_-461+3020insA (KRT10-AS1)	XP_005257146.1:n.-461+3019_-461+3020insA
XM_005257343.3:c.358_359insT (KRT10)	XP_005257400.1:p.Gly120ValfsTer27
XM_017024253.1:c.-414+3019_-414+3020insA (KRT10-AS1)	XP_016879742.1:n.-414+3019_-414+3020insA
NM_000421.4:c.358_359insT (KRT10)	NP_000412.3:p.Gly120ValfsTer27
NR_160886.1:n.95+2948_95+2949insA (KRT10-AS1)
NR_160887.1:n.26+3057_26+3058insA (KRT10-AS1)
NR_160888.1:n.64+3019_64+3020insA (KRT10-AS1)
NM_000421.5:c.358_359insT (KRT10) MANE Select	NP_000412.4:p.Gly120ValfsTer27
NM_001379366.1:c.358_359insT (KRT10)	NP_001366295.1:p.Gly120ValfsTer27