Canonical Allele Identifier: CA2260099841
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612558C= , CM000679.2:g.41612558C= GRCh38
NC_000017.10:g.39768810C= , CM000679.1:g.39768810C= GRCh37
NC_000017.9:g.37022336C= NCBI36
NG_008301.1:g.5270G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.131G= MANE Select ENSP00000301653.3:p.Ser44=
ENST00000301653.8:c.131G= ENSP00000301653.3:p.Ser44=
ENST00000588319.1:n.208G=
ENST00000590990.1:c.131G= ENSP00000467105.1:p.Ser44=
ENST00000593067.1:c.-313+232G= ENSP00000467124.1:n.-313+232G=
NM_005557.3:c.131G= NP_005548.2:p.Ser44=
NM_005557.4:c.131G= MANE Select NP_005548.2:p.Ser44=