Canonical Allele Identifier: CA2260099635
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612206G= , CM000679.2:g.41612206G= GRCh38
NC_000017.10:g.39768458G= , CM000679.1:g.39768458G= GRCh37
NC_000017.9:g.37021984G= NCBI36
NG_008301.1:g.5622C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.483C= MANE Select ENSP00000301653.3:p.Ile161=
ENST00000301653.8:c.483C= ENSP00000301653.3:p.Ile161=
ENST00000588319.1:n.560C=
ENST00000593067.1:c.-232C= ENSP00000467124.1:n.-232C=
NM_005557.3:c.483C= NP_005548.2:p.Ile161=
NM_005557.4:c.483C= MANE Select NP_005548.2:p.Ile161=