Canonical Allele Identifier: CA8548016
Gene: KRT10 HGNC NCBI

Linked Data

dbSNP Id: rs1567707158
ExAC: 17:38975307 TGCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCC / T
gnomAD v2: 17-38975307-TGCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCC-T
gnomAD v4: 17-40819055-TGCCGCCGTGGCCGCCGCCGTGGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCC-T
MyVariant Identifiers: chr17:g.38975308_38975361del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819064_40819117del , CM000679.2:g.40819064_40819117del GRCh38
NC_000017.10:g.38975316_38975369del , CM000679.1:g.38975316_38975369del GRCh37
NC_000017.9:g.36228842_36228895del NCBI36
NG_008405.1:g.8503_8556del
NG_033147.1:g.4973_5026del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1426_1479del MANE Select ENSP00000269576.5:p.Gly476_Gly493del
ENST00000635956.2:c.1426_1479del ENSP00000490524.2:p.Gly476_Gly493del
ENST00000269576.5:c.1426_1479del ENSP00000269576.5:p.Gly476_Gly493del
NM_000421.3:c.1426_1479del NP_000412.3:p.Gly476_Gly493del
XM_005257343.2:c.1426_1479del XP_005257400.1:p.Gly476_Gly493del
XM_005257343.3:c.1426_1479del XP_005257400.1:p.Gly476_Gly493del
NM_000421.4:c.1426_1479del NP_000412.3:p.Gly476_Gly493del
NM_000421.5:c.1426_1479del MANE Select NP_000412.4:p.Gly476_Gly493del
NM_001379366.1:c.1426_1479del NP_001366295.1:p.Gly476_Gly493del
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