Canonical Allele Identifier: CA2809476181

Gene: KRT10 KRT10-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822208_40822214del , CM000679.2:g.40822208_40822214del	GRCh38
NC_000017.10:g.38978460_38978466del , CM000679.1:g.38978460_38978466del	GRCh37
NC_000017.9:g.36231986_36231992del	NCBI36
NG_008405.1:g.5398_5404del
NG_033147.1:g.8117_8123del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.372_378del (KRT10) MANE Select	ENSP00000269576.5:p.Gly125LeufsTer22
ENST00000635956.2:c.372_378del (KRT10)	ENSP00000490524.2:p.Gly125LeufsTer22
ENST00000269576.5:c.372_378del (KRT10)	ENSP00000269576.5:p.Gly125LeufsTer22
ENST00000301665.7:c.-221+3000_-221+3006del (KRT10-AS1)	ENSP00000301665.3:n.-221+3000_-221+3006del
ENST00000436612.5:c.-221+3038_-221+3044del (KRT10-AS1)	ENSP00000390036.1:n.-221+3038_-221+3044del
ENST00000496847.1:n.49+3000_49+3006del (KRT10-AS1)
ENST00000622451.1:c.-221+2929_-221+2935del (KRT10-AS1)	ENSP00000482364.1:n.-221+2929_-221+2935del
NM_000421.3:c.372_378del (KRT10)	NP_000412.3:p.Gly125LeufsTer22
NM_001195386.1:c.-221+2929_-221+2935del (KRT10-AS1)	NP_001182315.1:n.-221+2929_-221+2935del
NM_001195387.1:c.-221+3038_-221+3044del (KRT10-AS1)	NP_001182316.1:n.-221+3038_-221+3044del
NM_145274.3:c.-221+3000_-221+3006del (KRT10-AS1)	NP_660317.2:n.-221+3000_-221+3006del
XM_005257343.2:c.372_378del (KRT10)	XP_005257400.1:p.Gly125LeufsTer22
XM_005257089.4:c.-461+3000_-461+3006del (KRT10-AS1)	XP_005257146.1:n.-461+3000_-461+3006del
XM_005257343.3:c.372_378del (KRT10)	XP_005257400.1:p.Gly125LeufsTer22
XM_017024253.1:c.-414+3000_-414+3006del (KRT10-AS1)	XP_016879742.1:n.-414+3000_-414+3006del
NM_000421.4:c.372_378del (KRT10)	NP_000412.3:p.Gly125LeufsTer22
NR_160886.1:n.95+2929_95+2935del (KRT10-AS1)
NR_160887.1:n.26+3038_26+3044del (KRT10-AS1)
NR_160888.1:n.64+3000_64+3006del (KRT10-AS1)
NM_000421.5:c.372_378del (KRT10) MANE Select	NP_000412.4:p.Gly125LeufsTer22
NM_001379366.1:c.372_378del (KRT10)	NP_001366295.1:p.Gly125LeufsTer22