Canonical Allele Identifier: CA2260099731
Gene: KRT16 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612372A= , CM000679.2:g.41612372A= GRCh38
NC_000017.10:g.39768624A= , CM000679.1:g.39768624A= GRCh37
NC_000017.9:g.37022150A= NCBI36
NG_008301.1:g.5456T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.317T= MANE Select ENSP00000301653.3:p.Phe106=
ENST00000301653.8:c.317T= ENSP00000301653.3:p.Phe106=
ENST00000588319.1:n.394T=
ENST00000593067.1:c.-312-86T= ENSP00000467124.1:n.-312-86T=
NM_005557.3:c.317T= NP_005548.2:p.Phe106=
NM_005557.4:c.317T= MANE Select NP_005548.2:p.Phe106=
Search 100 bp 5'
Search 100 bp 3'