Canonical Allele Identifier: CA2259725511

Gene: KRT10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819064_40819118delinsGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTA , CM000679.2:g.40819064_40819118delinsGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTA	GRCh38
NC_000017.10:g.38975316_38975370delinsGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTA , CM000679.1:g.38975316_38975370delinsGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTA	GRCh37
NC_000017.9:g.36228842_36228896delinsGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTA	NCBI36
NG_008405.1:g.8494_8548delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC
NG_033147.1:g.4973_5027delinsGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000269576.6:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC MANE Select	ENSP00000269576.5:p.Tyr473=
ENST00000635956.2:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC	ENSP00000490524.2:p.Tyr473=
ENST00000269576.5:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC	ENSP00000269576.5:p.Tyr473=
NM_000421.3:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC	NP_000412.3:p.Tyr473=
XM_005257343.2:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC	XP_005257400.1:p.Tyr473=
XM_005257343.3:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC	XP_005257400.1:p.Tyr473=
NM_000421.4:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC	NP_000412.3:p.Tyr473=
NM_000421.5:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC MANE Select	NP_000412.4:p.Tyr473=
NM_001379366.1:c.1417_1471delinsTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGCC	NP_001366295.1:p.Tyr473=