Canonical Allele Identifier: CA2260099790
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612489C= , CM000679.2:g.41612489C= GRCh38
NC_000017.10:g.39768741C= , CM000679.1:g.39768741C= GRCh37
NC_000017.9:g.37022267C= NCBI36
NG_008301.1:g.5339G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.200G= MANE Select ENSP00000301653.3:p.Gly67=
ENST00000301653.8:c.200G= ENSP00000301653.3:p.Gly67=
ENST00000588319.1:n.277G=
ENST00000593067.1:c.-312-203G= ENSP00000467124.1:n.-312-203G=
NM_005557.3:c.200G= NP_005548.2:p.Gly67=
NM_005557.4:c.200G= MANE Select NP_005548.2:p.Gly67=