Canonical Allele Identifier: CA2260099795
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612493C= , CM000679.2:g.41612493C= GRCh38
NC_000017.10:g.39768745C= , CM000679.1:g.39768745C= GRCh37
NC_000017.9:g.37022271C= NCBI36
NG_008301.1:g.5335G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.196G= MANE Select ENSP00000301653.3:p.Gly66=
ENST00000301653.8:c.196G= ENSP00000301653.3:p.Gly66=
ENST00000588319.1:n.273G=
ENST00000593067.1:c.-312-207G= ENSP00000467124.1:n.-312-207G=
NM_005557.3:c.196G= NP_005548.2:p.Gly66=
NM_005557.4:c.196G= MANE Select NP_005548.2:p.Gly66=