Canonical Allele Identifier: CA2552150698

Gene: KRT10 KRT10-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822225_40822308del , CM000679.2:g.40822225_40822308del	GRCh38
NC_000017.10:g.38978477_38978560del , CM000679.1:g.38978477_38978560del	GRCh37
NC_000017.9:g.36232003_36232086del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.288_371del (KRT10) MANE Select	ENSP00000269576.5:p.Ser97_Gly124del
ENST00000635956.2:c.288_371del (KRT10)	ENSP00000490524.2:p.Ser97_Gly124del
ENST00000269576.5:c.288_371del (KRT10)	ENSP00000269576.5:p.Ser97_Gly124del
ENST00000301665.7:c.-221+3017_-221+3100del (KRT10-AS1)	ENSP00000301665.3:n.-221+3017_-221+3100del
ENST00000436612.5:c.-221+3055_-221+3138del (KRT10-AS1)	ENSP00000390036.1:n.-221+3055_-221+3138del
ENST00000496847.1:n.49+3017_49+3100del (KRT10-AS1)
ENST00000622451.1:c.-221+2946_-221+3029del (KRT10-AS1)	ENSP00000482364.1:n.-221+2946_-221+3029del
NM_001195386.1:c.-221+2946_-221+3029del (KRT10-AS1)	NP_001182315.1:n.-221+2946_-221+3029del
NM_001195387.1:c.-221+3055_-221+3138del (KRT10-AS1)	NP_001182316.1:n.-221+3055_-221+3138del
NM_145274.3:c.-221+3017_-221+3100del (KRT10-AS1)	NP_660317.2:n.-221+3017_-221+3100del
XM_005257343.2:c.288_371del (KRT10)	XP_005257400.1:p.Ser97_Gly124del
XM_005257089.4:c.-461+3017_-461+3100del (KRT10-AS1)	XP_005257146.1:n.-461+3017_-461+3100del
XM_005257343.3:c.288_371del (KRT10)	XP_005257400.1:p.Ser97_Gly124del
XM_017024253.1:c.-414+3017_-414+3100del (KRT10-AS1)	XP_016879742.1:n.-414+3017_-414+3100del
NR_160886.1:n.95+2946_95+3029del (KRT10-AS1)
NR_160887.1:n.26+3055_26+3138del (KRT10-AS1)
NR_160888.1:n.64+3017_64+3100del (KRT10-AS1)
NM_000421.5:c.288_371del (KRT10) MANE Select	NP_000412.4:p.Ser97_Gly124del
NM_001379366.1:c.288_371del (KRT10)	NP_001366295.1:p.Ser97_Gly124del