Canonical Allele Identifier: CA2259725258

Gene: KRT10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40818966_40818993delinsGCCGTGGCCGCCGCTGGAGCTTCCGCCC , CM000679.2:g.40818966_40818993delinsGCCGTGGCCGCCGCTGGAGCTTCCGCCC	GRCh38
NC_000017.10:g.38975218_38975245delinsGCCGTGGCCGCCGCTGGAGCTTCCGCCC , CM000679.1:g.38975218_38975245delinsGCCGTGGCCGCCGCTGGAGCTTCCGCCC	GRCh37
NC_000017.9:g.36228744_36228771delinsGCCGTGGCCGCCGCTGGAGCTTCCGCCC	NCBI36
NG_008405.1:g.8619_8646delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC
NG_033147.1:g.4875_4902delinsGCCGTGGCCGCCGCTGGAGCTTCCGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC MANE Select	ENSP00000269576.5:p.Gly514=
ENST00000635956.2:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC	ENSP00000490524.2:p.Gly514=
ENST00000269576.5:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC	ENSP00000269576.5:p.Gly514=
NM_000421.3:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC	NP_000412.3:p.Gly514=
XM_005257343.2:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC	XP_005257400.1:p.Gly514=
XM_005257343.3:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC	XP_005257400.1:p.Gly514=
NM_000421.4:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC	NP_000412.3:p.Gly514=
NM_000421.5:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC MANE Select	NP_000412.4:p.Gly514=
NM_001379366.1:c.1542_1569delinsGGGCGGAAGCTCCAGCGGCGGCCACGGC	NP_001366295.1:p.Gly514=