Canonical Allele Identifier: CA983759340
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908255177
gnomAD v3: 17-41612743-C-A
gnomAD v4: 17-41612743-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612743C>A , CM000679.2:g.41612743C>A GRCh38
NC_000017.10:g.39768995C>A , CM000679.1:g.39768995C>A GRCh37
NC_000017.9:g.37022521C>A NCBI36
NG_008301.1:g.5085G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-55G>T MANE Select ENSP00000301653.3:n.-55G>T
ENST00000301653.8:c.-55G>T ENSP00000301653.3:n.-55G>T
ENST00000588319.1:n.23G>T
ENST00000590990.1:c.-36-19G>T ENSP00000467105.1:n.-36-19G>T
ENST00000593067.1:c.-313+47G>T ENSP00000467124.1:n.-313+47G>T
NM_005557.3:c.-55G>T NP_005548.2:n.-55G>T
NM_005557.4:c.-55G>T MANE Select NP_005548.2:n.-55G>T
Search 100 bp 5'
Search 100 bp 3'