Canonical Allele Identifier: CA2260099960
Gene: KRT16 HGNC NCBI
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-55G= MANE Select ENSP00000301653.3:n.-55G=
ENST00000301653.8:c.-55G= ENSP00000301653.3:n.-55G=
ENST00000588319.1:n.23G=
ENST00000590990.1:c.-36-19G= ENSP00000467105.1:n.-36-19G=
ENST00000593067.1:c.-313+47G= ENSP00000467124.1:n.-313+47G=
NM_005557.3:c.-55G= NP_005548.2:n.-55G=
NM_005557.4:c.-55G= MANE Select NP_005548.2:n.-55G=
Search 100 bp 5'
Search 100 bp 3'