Canonical Allele Identifier: CA399496347
Gene: KRT16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612552T>A , CM000679.2:g.41612552T>A GRCh38
NC_000017.10:g.39768804T>A , CM000679.1:g.39768804T>A GRCh37
NC_000017.9:g.37022330T>A NCBI36
NG_008301.1:g.5276A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.137A>T MANE Select ENSP00000301653.3:p.Tyr46Phe
ENST00000301653.8:c.137A>T ENSP00000301653.3:p.Tyr46Phe
ENST00000588319.1:n.214A>T
ENST00000590990.1:c.137A>T ENSP00000467105.1:p.Tyr46Phe
ENST00000593067.1:c.-313+238A>T ENSP00000467124.1:n.-313+238A>T
NM_005557.3:c.137A>T NP_005548.2:p.Tyr46Phe
NM_005557.4:c.137A>T MANE Select NP_005548.2:p.Tyr46Phe