Canonical Allele Identifier: CA2259725515
Gene: KRT10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819065_40819146delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT , CM000679.2:g.40819065_40819146delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT GRCh38
NC_000017.10:g.38975317_38975398delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT , CM000679.1:g.38975317_38975398delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT GRCh37
NC_000017.9:g.36228843_36228924delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT NCBI36
NG_008405.1:g.8466_8547delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC
NG_033147.1:g.4974_5055delinsGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCGCCGTAGCCGCCGCCGAAACTTCCGCCGCCGCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC MANE Select ENSP00000269576.5:p.Gly463=
ENST00000635956.2:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC ENSP00000490524.2:p.Gly463=
ENST00000269576.5:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC ENSP00000269576.5:p.Gly463=
NM_000421.3:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC NP_000412.3:p.Gly463=
XM_005257343.2:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC XP_005257400.1:p.Gly463=
XM_005257343.3:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC XP_005257400.1:p.Gly463=
NM_000421.4:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC NP_000412.3:p.Gly463=
NM_000421.5:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC MANE Select NP_000412.4:p.Gly463=
NM_001379366.1:c.1389_1470delinsACGCGGCGGCGGAAGTTTCGGCGGCGGCTACGGCGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCCACGGCGGCGGC NP_001366295.1:p.Gly463=