Canonical Allele Identifier: CA8548002

Gene: KRT10

Linked Data

• ExAC: 17:38975284 GCCTCCGTAGCCGCCGCCGGAACTGCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCT / G
• MyVariant Identifiers: chr17:g.38975285_38975358del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819033_40819106del , CM000679.2:g.40819033_40819106del	GRCh38
NC_000017.10:g.38975285_38975358del , CM000679.1:g.38975285_38975358del	GRCh37
NC_000017.9:g.36228811_36228884del	NCBI36
NG_008405.1:g.8506_8579del
NG_033147.1:g.4942_5015del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1429_1502del MANE Select	ENSP00000269576.5:p.Ser477ArgfsTer?
ENST00000635956.2:c.1429_1502del	ENSP00000490524.2:p.Ser477ArgfsTer?
ENST00000269576.5:c.1429_1502del	ENSP00000269576.5:p.Ser477ArgfsTer?
NM_000421.3:c.1429_1502del	NP_000412.3:p.Ser477ArgfsTer?
XM_005257343.2:c.1429_1502del	XP_005257400.1:p.Ser477ArgfsTer?
XM_005257343.3:c.1429_1502del	XP_005257400.1:p.Ser477ArgfsTer?
NM_000421.4:c.1429_1502del	NP_000412.3:p.Ser477ArgfsTer?
NM_000421.5:c.1429_1502del MANE Select	NP_000412.4:p.Ser477ArgfsTer?
NM_001379366.1:c.1429_1502del	NP_001366295.1:p.Ser477ArgfsTer?