Canonical Allele Identifier: CA2637770988

Gene: KRT10 KRT10-AS1

Linked Data

• gnomAD v4: 17-40822283-G-GCTGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822283_40822284insCTGCC , CM000679.2:g.40822283_40822284insCTGCC	GRCh38
NC_000017.10:g.38978535_38978536insCTGCC , CM000679.1:g.38978535_38978536insCTGCC	GRCh37
NC_000017.9:g.36232061_36232062insCTGCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.302_303insGGCAG (KRT10) MANE Select	ENSP00000269576.5:p.Ile101MetfsTer?
ENST00000635956.2:c.302_303insGGCAG (KRT10)	ENSP00000490524.2:p.Ile101MetfsTer?
ENST00000269576.5:c.302_303insGGCAG (KRT10)	ENSP00000269576.5:p.Ile101MetfsTer?
ENST00000301665.7:c.-221+3075_-221+3076insCTGCC (KRT10-AS1)	ENSP00000301665.3:n.-221+3075_-221+3076insCTGCC
ENST00000436612.5:c.-221+3113_-221+3114insCTGCC (KRT10-AS1)	ENSP00000390036.1:n.-221+3113_-221+3114insCTGCC
ENST00000496847.1:n.49+3075_49+3076insCTGCC (KRT10-AS1)
ENST00000622451.1:c.-221+3004_-221+3005insCTGCC (KRT10-AS1)	ENSP00000482364.1:n.-221+3004_-221+3005insCTGCC
NM_001195386.1:c.-221+3004_-221+3005insCTGCC (KRT10-AS1)	NP_001182315.1:n.-221+3004_-221+3005insCTGCC
NM_001195387.1:c.-221+3113_-221+3114insCTGCC (KRT10-AS1)	NP_001182316.1:n.-221+3113_-221+3114insCTGCC
NM_145274.3:c.-221+3075_-221+3076insCTGCC (KRT10-AS1)	NP_660317.2:n.-221+3075_-221+3076insCTGCC
XM_005257343.2:c.302_303insGGCAG (KRT10)	XP_005257400.1:p.Ile101MetfsTer?
XM_005257089.4:c.-461+3075_-461+3076insCTGCC (KRT10-AS1)	XP_005257146.1:n.-461+3075_-461+3076insCTGCC
XM_005257343.3:c.302_303insGGCAG (KRT10)	XP_005257400.1:p.Ile101MetfsTer?
XM_017024253.1:c.-414+3075_-414+3076insCTGCC (KRT10-AS1)	XP_016879742.1:n.-414+3075_-414+3076insCTGCC
NR_160886.1:n.95+3004_95+3005insCTGCC (KRT10-AS1)
NR_160887.1:n.26+3113_26+3114insCTGCC (KRT10-AS1)
NR_160888.1:n.64+3075_64+3076insCTGCC (KRT10-AS1)
NM_000421.5:c.302_303insGGCAG (KRT10) MANE Select	NP_000412.4:p.Ile101MetfsTer?
NM_001379366.1:c.302_303insGGCAG (KRT10)	NP_001366295.1:p.Ile101MetfsTer?