Canonical Allele Identifier: CA919840251

Gene: KRT10 KRT10-AS1

Linked Data

• dbSNP Id: rs1597822220

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822019_40822020del , CM000679.2:g.40822019_40822020del	GRCh38
NC_000017.10:g.38978271_38978272del , CM000679.1:g.38978271_38978272del	GRCh37
NC_000017.9:g.36231797_36231798del	NCBI36
NG_008405.1:g.5592_5593del
NG_033147.1:g.7928_7929del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.566_567del (KRT10) MANE Select	ENSP00000269576.5:p.His189ProfsTer6
ENST00000635956.2:c.566_567del (KRT10)	ENSP00000490524.2:p.His189ProfsTer6
ENST00000269576.5:c.566_567del (KRT10)	ENSP00000269576.5:p.His189ProfsTer6
ENST00000301665.7:c.-221+2811_-221+2812del (KRT10-AS1)	ENSP00000301665.3:n.-221+2811_-221+2812del
ENST00000436612.5:c.-221+2849_-221+2850del (KRT10-AS1)	ENSP00000390036.1:n.-221+2849_-221+2850del
ENST00000496847.1:n.49+2811_49+2812del (KRT10-AS1)
ENST00000622451.1:c.-221+2740_-221+2741del (KRT10-AS1)	ENSP00000482364.1:n.-221+2740_-221+2741del
NM_000421.3:c.566_567del (KRT10)	NP_000412.3:p.His189ProfsTer6
NM_001195386.1:c.-221+2740_-221+2741del (KRT10-AS1)	NP_001182315.1:n.-221+2740_-221+2741del
NM_001195387.1:c.-221+2849_-221+2850del (KRT10-AS1)	NP_001182316.1:n.-221+2849_-221+2850del
NM_145274.3:c.-221+2811_-221+2812del (KRT10-AS1)	NP_660317.2:n.-221+2811_-221+2812del
XM_005257343.2:c.566_567del (KRT10)	XP_005257400.1:p.His189ProfsTer6
XM_005257089.4:c.-461+2811_-461+2812del (KRT10-AS1)	XP_005257146.1:n.-461+2811_-461+2812del
XM_005257343.3:c.566_567del (KRT10)	XP_005257400.1:p.His189ProfsTer6
XM_017024253.1:c.-414+2811_-414+2812del (KRT10-AS1)	XP_016879742.1:n.-414+2811_-414+2812del
NM_000421.4:c.566_567del (KRT10)	NP_000412.3:p.His189ProfsTer6
NR_160886.1:n.95+2740_95+2741del (KRT10-AS1)
NR_160887.1:n.26+2849_26+2850del (KRT10-AS1)
NR_160888.1:n.64+2811_64+2812del (KRT10-AS1)
NM_000421.5:c.566_567del (KRT10) MANE Select	NP_000412.4:p.His189ProfsTer6
NM_001379366.1:c.566_567del (KRT10)	NP_001366295.1:p.His189ProfsTer6