Canonical Allele Identifier: CA2637838185
Gene: KRT16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612550del , CM000679.2:g.41612550del GRCh38
NC_000017.10:g.39768802del , CM000679.1:g.39768802del GRCh37
NC_000017.9:g.37022328del NCBI36
NG_008301.1:g.5282del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.143del MANE Select ENSP00000301653.3:p.Gly48AlafsTer?
ENST00000301653.8:c.143del ENSP00000301653.3:p.Gly48AlafsTer?
ENST00000588319.1:n.220del
ENST00000590990.1:c.143del ENSP00000467105.1:p.Gly48AlafsTer?
ENST00000593067.1:c.-313+244del ENSP00000467124.1:n.-313+244del
NM_005557.3:c.143del NP_005548.2:p.Gly48AlafsTer?
NM_005557.4:c.143del MANE Select NP_005548.2:p.Gly48AlafsTer?