Canonical Allele Identifier: CA399495935
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1555573913
gnomAD v2: 17-39768743-GC-G
gnomAD v3: 17-41612491-GC-G
gnomAD v4: 17-41612491-GC-G
COSMIC: COSM1383214
MyVariant Identifiers: chr17:g.39768744del (hg19) chr17:g.41612493del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612497del , CM000679.2:g.41612497del GRCh38
NC_000017.10:g.39768749del , CM000679.1:g.39768749del GRCh37
NC_000017.9:g.37022275del NCBI36
NG_008301.1:g.5336del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.197del MANE Select ENSP00000301653.3:p.Gly66AlafsTer?
ENST00000301653.8:c.197del ENSP00000301653.3:p.Gly66AlafsTer?
ENST00000588319.1:n.274del
ENST00000593067.1:c.-312-206del ENSP00000467124.1:n.-312-206del
NM_005557.3:c.197del NP_005548.2:p.Gly66AlafsTer?
NM_005557.4:c.197del MANE Select NP_005548.2:p.Gly66AlafsTer?
Search 100 bp 5'
Search 100 bp 3'