Canonical Allele Identifier: CA290665068
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs796162362
gnomAD v2: 17-39740285-TTCTCTCTCTCTCTCTCAATC-T
gnomAD v3: 17-41584033-TTCTCTCTCTCTCTCTCAATC-T
gnomAD v4: 17-41584033-TTCTCTCTCTCTCTCTCAATC-T
MyVariant Identifiers: chr17:g.39740290_39740309del (hg19) chr17:g.39740286_39740305del (hg19) chr17:g.41584038_41584057del (hg38) chr17:g.41584034_41584053del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584050_41584069del , CM000679.2:g.41584050_41584069del GRCh38
NC_000017.10:g.39740302_39740321del , CM000679.1:g.39740302_39740321del GRCh37
NC_000017.9:g.36993828_36993847del NCBI36
NG_008624.1:g.7843_7862del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-132_766-113del MANE Select ENSP00000167586.6:n.766-132_766-113del
ENST00000167586.6:c.766-132_766-113del ENSP00000167586.6:n.766-132_766-113del
ENST00000476662.1:n.216-132_216-113del
NM_000526.4:c.766-132_766-113del NP_000517.2:n.766-132_766-113del
NM_000526.5:c.766-132_766-113del MANE Select NP_000517.3:n.766-132_766-113del
Search 100 bp 5'
Search 100 bp 3'