Canonical Allele Identifier: CA8563245
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs752556556
ExAC: 17:39768403 C / CA
gnomAD v2: 17-39768403-C-CA
gnomAD v3: 17-41612151-C-CA
gnomAD v4: 17-41612151-C-CA
MyVariant Identifiers: chr17:g.39768403_39768404insA (hg19) chr17:g.41612151_41612152insA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612152dup , CM000679.2:g.41612152dup GRCh38
NC_000017.10:g.39768404dup , CM000679.1:g.39768404dup GRCh37
NC_000017.9:g.37021930dup NCBI36
NG_008301.1:g.5676dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.531+6dup MANE Select ENSP00000301653.3:n.531+6dup
ENST00000301653.8:c.531+6dup ENSP00000301653.3:n.531+6dup
ENST00000588319.1:n.614dup
ENST00000593067.1:c.-184+6dup ENSP00000467124.1:n.-184+6dup
NM_005557.3:c.531+6dup NP_005548.2:n.531+6dup
NM_005557.4:c.531+6dup MANE Select NP_005548.2:n.531+6dup
Search 100 bp 5'
Search 100 bp 3'