Canonical Allele Identifier: CA2259725264

Gene: KRT10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40818971_40818998delinsGGCCGCCGCTGGAGCTTCCGCCCCCGTA , CM000679.2:g.40818971_40818998delinsGGCCGCCGCTGGAGCTTCCGCCCCCGTA	GRCh38
NC_000017.10:g.38975223_38975250delinsGGCCGCCGCTGGAGCTTCCGCCCCCGTA , CM000679.1:g.38975223_38975250delinsGGCCGCCGCTGGAGCTTCCGCCCCCGTA	GRCh37
NC_000017.9:g.36228749_36228776delinsGGCCGCCGCTGGAGCTTCCGCCCCCGTA	NCBI36
NG_008405.1:g.8614_8641delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC
NG_033147.1:g.4880_4907delinsGGCCGCCGCTGGAGCTTCCGCCCCCGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000269576.6:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC MANE Select	ENSP00000269576.5:p.Tyr513=
ENST00000635956.2:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC	ENSP00000490524.2:p.Tyr513=
ENST00000269576.5:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC	ENSP00000269576.5:p.Tyr513=
NM_000421.3:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC	NP_000412.3:p.Tyr513=
XM_005257343.2:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC	XP_005257400.1:p.Tyr513=
XM_005257343.3:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC	XP_005257400.1:p.Tyr513=
NM_000421.4:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC	NP_000412.3:p.Tyr513=
NM_000421.5:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC MANE Select	NP_000412.4:p.Tyr513=
NM_001379366.1:c.1537_1564delinsTACGGGGGCGGAAGCTCCAGCGGCGGCC	NP_001366295.1:p.Tyr513=