Canonical Allele Identifier: CA2260099620
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612164C= , CM000679.2:g.41612164C= GRCh38
NC_000017.10:g.39768416C= , CM000679.1:g.39768416C= GRCh37
NC_000017.9:g.37021942C= NCBI36
NG_008301.1:g.5664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.525G= MANE Select ENSP00000301653.3:p.Arg175=
ENST00000301653.8:c.525G= ENSP00000301653.3:p.Arg175=
ENST00000588319.1:n.602G=
ENST00000593067.1:c.-190G= ENSP00000467124.1:n.-190G=
NM_005557.3:c.525G= NP_005548.2:p.Arg175=
NM_005557.4:c.525G= MANE Select NP_005548.2:p.Arg175=