Canonical Allele Identifier: CA2259725591

Gene: KRT10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819077_40819092delinsGCCGCCGCCGGAGCTT , CM000679.2:g.40819077_40819092delinsGCCGCCGCCGGAGCTT	GRCh38
NC_000017.10:g.38975329_38975344delinsGCCGCCGCCGGAGCTT , CM000679.1:g.38975329_38975344delinsGCCGCCGCCGGAGCTT	GRCh37
NC_000017.9:g.36228855_36228870delinsGCCGCCGCCGGAGCTT	NCBI36
NG_008405.1:g.8520_8535delinsAAGCTCCGGCGGCGGC
NG_033147.1:g.4986_5001delinsGCCGCCGCCGGAGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1443_1458delinsAAGCTCCGGCGGCGGC MANE Select	ENSP00000269576.5:p.Gly481=
ENST00000635956.2:c.1443_1458delinsAAGCTCCGGCGGCGGC	ENSP00000490524.2:p.Gly481=
ENST00000269576.5:c.1443_1458delinsAAGCTCCGGCGGCGGC	ENSP00000269576.5:p.Gly481=
NM_000421.3:c.1443_1458delinsAAGCTCCGGCGGCGGC	NP_000412.3:p.Gly481=
XM_005257343.2:c.1443_1458delinsAAGCTCCGGCGGCGGC	XP_005257400.1:p.Gly481=
XM_005257343.3:c.1443_1458delinsAAGCTCCGGCGGCGGC	XP_005257400.1:p.Gly481=
NM_000421.4:c.1443_1458delinsAAGCTCCGGCGGCGGC	NP_000412.3:p.Gly481=
NM_000421.5:c.1443_1458delinsAAGCTCCGGCGGCGGC MANE Select	NP_000412.4:p.Gly481=
NM_001379366.1:c.1443_1458delinsAAGCTCCGGCGGCGGC	NP_001366295.1:p.Gly481=