Canonical Allele Identifier: CA983720479

Gene: KRT10

Linked Data

• dbSNP Id: rs1905215214
• gnomAD v3: 17-40819075-TGGCCGCCGCCGGAGCTTCCGCCGCC-T
• gnomAD v4: 17-40819075-TGGCCGCCGCCGGAGCTTCCGCCGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40819078_40819102del , CM000679.2:g.40819078_40819102del	GRCh38
NC_000017.10:g.38975330_38975354del , CM000679.1:g.38975330_38975354del	GRCh37
NC_000017.9:g.36228856_36228880del	NCBI36
NG_008405.1:g.8512_8536del
NG_033147.1:g.4987_5011del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269576.6:c.1435_1459del MANE Select	ENSP00000269576.5:p.Gly479ThrfsTer?
ENST00000635956.2:c.1435_1459del	ENSP00000490524.2:p.Gly479ThrfsTer?
ENST00000269576.5:c.1435_1459del	ENSP00000269576.5:p.Gly479ThrfsTer?
NM_000421.3:c.1435_1459del	NP_000412.3:p.Gly479ThrfsTer?
XM_005257343.2:c.1435_1459del	XP_005257400.1:p.Gly479ThrfsTer?
XM_005257343.3:c.1435_1459del	XP_005257400.1:p.Gly479ThrfsTer?
NM_000421.4:c.1435_1459del	NP_000412.3:p.Gly479ThrfsTer?
NM_000421.5:c.1435_1459del MANE Select	NP_000412.4:p.Gly479ThrfsTer?
NM_001379366.1:c.1435_1459del	NP_001366295.1:p.Gly479ThrfsTer?