Canonical Allele Identifier: CA2260099679
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612289T= , CM000679.2:g.41612289T= GRCh38
NC_000017.10:g.39768541T= , CM000679.1:g.39768541T= GRCh37
NC_000017.9:g.37022067T= NCBI36
NG_008301.1:g.5539A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.400A= MANE Select ENSP00000301653.3:p.Lys134=
ENST00000301653.8:c.400A= ENSP00000301653.3:p.Lys134=
ENST00000588319.1:n.477A=
ENST00000593067.1:c.-312-3A= ENSP00000467124.1:n.-312-3A=
NM_005557.3:c.400A= NP_005548.2:p.Lys134=
NM_005557.4:c.400A= MANE Select NP_005548.2:p.Lys134=