Canonical Allele Identifier: CA2809496613
Gene: KRT16 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612751G>T , CM000679.2:g.41612751G>T GRCh38
NC_000017.10:g.39769003G>T , CM000679.1:g.39769003G>T GRCh37
NC_000017.9:g.37022529G>T NCBI36
NG_008301.1:g.5077C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-63C>A MANE Select ENSP00000301653.3:n.-63C>A
ENST00000301653.8:c.-63C>A ENSP00000301653.3:n.-63C>A
ENST00000588319.1:n.15C>A
ENST00000590990.1:c.-36-27C>A ENSP00000467105.1:n.-36-27C>A
ENST00000593067.1:c.-313+39C>A ENSP00000467124.1:n.-313+39C>A
NM_005557.3:c.-63C>A NP_005548.2:n.-63C>A
NM_005557.4:c.-63C>A MANE Select NP_005548.2:n.-63C>A
Search 100 bp 5'
Search 100 bp 3'