Canonical Allele Identifier: CA2259725519

Gene: KRT10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819065_40819107delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTT , CM000679.2:g.40819065_40819107delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTT	GRCh38
NC_000017.10:g.38975317_38975359delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTT , CM000679.1:g.38975317_38975359delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTT	GRCh37
NC_000017.9:g.36228843_36228885delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTT	NCBI36
NG_008405.1:g.8505_8547delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC
NG_033147.1:g.4974_5016delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC MANE Select	ENSP00000269576.5:p.Gly476=
ENST00000635956.2:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC	ENSP00000490524.2:p.Gly476=
ENST00000269576.5:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC	ENSP00000269576.5:p.Gly476=
NM_000421.3:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC	NP_000412.3:p.Gly476=
XM_005257343.2:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC	XP_005257400.1:p.Gly476=
XM_005257343.3:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC	XP_005257400.1:p.Gly476=
NM_000421.4:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC	NP_000412.3:p.Gly476=
NM_000421.5:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC MANE Select	NP_000412.4:p.Gly476=
NM_001379366.1:c.1428_1470delinsAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC	NP_001366295.1:p.Gly476=