Canonical Allele Identifier: CA2637768512

Gene: KRT10

Linked Data

• gnomAD v4: 17-40819064-GGCCGCCGCCGTGGCCGCCGCCGGAGCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819065_40819092del , CM000679.2:g.40819065_40819092del	GRCh38
NC_000017.10:g.38975317_38975344del , CM000679.1:g.38975317_38975344del	GRCh37
NC_000017.9:g.36228843_36228870del	NCBI36
NG_008405.1:g.8520_8547del
NG_033147.1:g.4974_5001del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269576.6:c.1443_1470del MANE Select	ENSP00000269576.5:p.Ser482ThrfsTer?
ENST00000635956.2:c.1443_1470del	ENSP00000490524.2:p.Ser482ThrfsTer?
ENST00000269576.5:c.1443_1470del	ENSP00000269576.5:p.Ser482ThrfsTer?
NM_000421.3:c.1443_1470del	NP_000412.3:p.Ser482ThrfsTer?
XM_005257343.2:c.1443_1470del	XP_005257400.1:p.Ser482ThrfsTer?
XM_005257343.3:c.1443_1470del	XP_005257400.1:p.Ser482ThrfsTer?
NM_000421.4:c.1443_1470del	NP_000412.3:p.Ser482ThrfsTer?
NM_000421.5:c.1443_1470del MANE Select	NP_000412.4:p.Ser482ThrfsTer?
NM_001379366.1:c.1443_1470del	NP_001366295.1:p.Ser482ThrfsTer?