Canonical Allele Identifier: CA2637771101

Gene: KRT10 KRT10-AS1

Linked Data

• gnomAD v4: 17-40822516-C-CTCCTCCTCCTCCTCCTCCACA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40822534_40822535insACATCCTCCTCCTCCTCCTCC , CM000679.2:g.40822534_40822535insACATCCTCCTCCTCCTCCTCC	GRCh38
NC_000017.10:g.38978786_38978787insACATCCTCCTCCTCCTCCTCC , CM000679.1:g.38978786_38978787insACATCCTCCTCCTCCTCCTCC	GRCh37
NC_000017.9:g.36232312_36232313insACATCCTCCTCCTCCTCCTCC	NCBI36
NG_008405.1:g.5095_5096insTGTGGAGGAGGAGGAGGAGGA
NG_033147.1:g.8443_8444insACATCCTCCTCCTCCTCCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10) MANE Select	ENSP00000269576.5:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly
ENST00000635956.2:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10)	ENSP00000490524.2:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly
ENST00000269576.5:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10)	ENSP00000269576.5:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly
ENST00000301665.7:c.-221+3326_-221+3327insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)	ENSP00000301665.3:n.-221+3326_-221+3327insACATCCTCCTCCTCCTCCT...
ENST00000436612.5:c.-221+3364_-221+3365insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)	ENSP00000390036.1:n.-221+3364_-221+3365insACATCCTCCTCCTCCTCCT...
ENST00000496847.1:n.49+3326_49+3327insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)
ENST00000622451.1:c.-221+3255_-221+3256insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)	ENSP00000482364.1:n.-221+3255_-221+3256insACATCCTCCTCCTCCTCCT...
NM_000421.3:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10)	NP_000412.3:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly
NM_001195386.1:c.-221+3255_-221+3256insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)	NP_001182315.1:n.-221+3255_-221+3256insACATCCTCCTCCTCCTCCTCC
NM_001195387.1:c.-221+3364_-221+3365insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)	NP_001182316.1:n.-221+3364_-221+3365insACATCCTCCTCCTCCTCCTCC
NM_145274.3:c.-221+3326_-221+3327insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)	NP_660317.2:n.-221+3326_-221+3327insACATCCTCCTCCTCCTCCTCC
XM_005257343.2:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10)	XP_005257400.1:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly
XM_005257089.4:c.-461+3326_-461+3327insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)	XP_005257146.1:n.-461+3326_-461+3327insACATCCTCCTCCTCCTCCTCC
XM_005257343.3:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10)	XP_005257400.1:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly
XM_017024253.1:c.-414+3326_-414+3327insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)	XP_016879742.1:n.-414+3326_-414+3327insACATCCTCCTCCTCCTCCTCC
NM_000421.4:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10)	NP_000412.3:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly
NR_160886.1:n.95+3255_95+3256insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)
NR_160887.1:n.26+3364_26+3365insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)
NR_160888.1:n.64+3326_64+3327insACATCCTCCTCCTCCTCCTCC (KRT10-AS1)
NM_000421.5:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10) MANE Select	NP_000412.4:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly
NM_001379366.1:c.69_70insTGTGGAGGAGGAGGAGGAGGA (KRT10)	NP_001366295.1:p.Gly23_Gly24insCysGlyGlyGlyGlyGlyGly