Canonical Allele Identifier: CA2259726747

Gene: KRT10 KRT10-AS1

Linked Data

• dbSNP Id: rs1905440842

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822206_40822217del , CM000679.2:g.40822206_40822217del	GRCh38
NC_000017.10:g.38978458_38978469del , CM000679.1:g.38978458_38978469del	GRCh37
NC_000017.9:g.36231984_36231995del	NCBI36
NG_008405.1:g.5401_5412del
NG_033147.1:g.8115_8126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.375_386del (KRT10) MANE Select	ENSP00000269576.5:p.Gly126_Gly129del
ENST00000635956.2:c.375_386del (KRT10)	ENSP00000490524.2:p.Gly126_Gly129del
ENST00000269576.5:c.375_386del (KRT10)	ENSP00000269576.5:p.Gly126_Gly129del
ENST00000301665.7:c.-221+2998_-221+3009del (KRT10-AS1)	ENSP00000301665.3:n.-221+2998_-221+3009del
ENST00000436612.5:c.-221+3036_-221+3047del (KRT10-AS1)	ENSP00000390036.1:n.-221+3036_-221+3047del
ENST00000496847.1:n.49+2998_49+3009del (KRT10-AS1)
ENST00000622451.1:c.-221+2927_-221+2938del (KRT10-AS1)	ENSP00000482364.1:n.-221+2927_-221+2938del
NM_000421.3:c.375_386del (KRT10)	NP_000412.3:p.Gly126_Gly129del
NM_001195386.1:c.-221+2927_-221+2938del (KRT10-AS1)	NP_001182315.1:n.-221+2927_-221+2938del
NM_001195387.1:c.-221+3036_-221+3047del (KRT10-AS1)	NP_001182316.1:n.-221+3036_-221+3047del
NM_145274.3:c.-221+2998_-221+3009del (KRT10-AS1)	NP_660317.2:n.-221+2998_-221+3009del
XM_005257343.2:c.375_386del (KRT10)	XP_005257400.1:p.Gly126_Gly129del
XM_005257089.4:c.-461+2998_-461+3009del (KRT10-AS1)	XP_005257146.1:n.-461+2998_-461+3009del
XM_005257343.3:c.375_386del (KRT10)	XP_005257400.1:p.Gly126_Gly129del
XM_017024253.1:c.-414+2998_-414+3009del (KRT10-AS1)	XP_016879742.1:n.-414+2998_-414+3009del
NM_000421.4:c.375_386del (KRT10)	NP_000412.3:p.Gly126_Gly129del
NR_160886.1:n.95+2927_95+2938del (KRT10-AS1)
NR_160887.1:n.26+3036_26+3047del (KRT10-AS1)
NR_160888.1:n.64+2998_64+3009del (KRT10-AS1)
NM_000421.5:c.375_386del (KRT10) MANE Select	NP_000412.4:p.Gly126_Gly129del
NM_001379366.1:c.375_386del (KRT10)	NP_001366295.1:p.Gly126_Gly129del