Canonical Allele Identifier: CA399495571
Gene: KRT16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612432T>A , CM000679.2:g.41612432T>A GRCh38
NC_000017.10:g.39768684T>A , CM000679.1:g.39768684T>A GRCh37
NC_000017.9:g.37022210T>A NCBI36
NG_008301.1:g.5396A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.257A>T MANE Select ENSP00000301653.3:p.Tyr86Phe
ENST00000301653.8:c.257A>T ENSP00000301653.3:p.Tyr86Phe
ENST00000588319.1:n.334A>T
ENST00000593067.1:c.-312-146A>T ENSP00000467124.1:n.-312-146A>T
NM_005557.3:c.257A>T NP_005548.2:p.Tyr86Phe
NM_005557.4:c.257A>T MANE Select NP_005548.2:p.Tyr86Phe