Canonical Allele Identifier: CA2260099889
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612628C= , CM000679.2:g.41612628C= GRCh38
NC_000017.10:g.39768880C= , CM000679.1:g.39768880C= GRCh37
NC_000017.9:g.37022406C= NCBI36
NG_008301.1:g.5200G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.61G= MANE Select ENSP00000301653.3:p.Gly21=
ENST00000301653.8:c.61G= ENSP00000301653.3:p.Gly21=
ENST00000588319.1:n.138G=
ENST00000590990.1:c.61G= ENSP00000467105.1:p.Gly21=
ENST00000593067.1:c.-313+162G= ENSP00000467124.1:n.-313+162G=
NM_005557.3:c.61G= NP_005548.2:p.Gly21=
NM_005557.4:c.61G= MANE Select NP_005548.2:p.Gly21=