Canonical Allele Identifier: CA8563250
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs756111023

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612160T>A , CM000679.2:g.41612160T>A GRCh38
NC_000017.10:g.39768412T>A , CM000679.1:g.39768412T>A GRCh37
NC_000017.9:g.37021938T>A NCBI36
NG_008301.1:g.5668A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.529A>T MANE Select ENSP00000301653.3:p.Lys177Ter
ENST00000301653.8:c.529A>T ENSP00000301653.3:p.Lys177Ter
ENST00000588319.1:n.606A>T
ENST00000593067.1:c.-186A>T ENSP00000467124.1:n.-186A>T
NM_005557.3:c.529A>T NP_005548.2:p.Lys177Ter
NM_005557.4:c.529A>T MANE Select NP_005548.2:p.Lys177Ter