Canonical Allele Identifier: CA2260099855
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612578T= , CM000679.2:g.41612578T= GRCh38
NC_000017.10:g.39768830T= , CM000679.1:g.39768830T= GRCh37
NC_000017.9:g.37022356T= NCBI36
NG_008301.1:g.5250A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.111A= MANE Select ENSP00000301653.3:p.Gly37=
ENST00000301653.8:c.111A= ENSP00000301653.3:p.Gly37=
ENST00000588319.1:n.188A=
ENST00000590990.1:c.111A= ENSP00000467105.1:p.Gly37=
ENST00000593067.1:c.-313+212A= ENSP00000467124.1:n.-313+212A=
NM_005557.3:c.111A= NP_005548.2:p.Gly37=
NM_005557.4:c.111A= MANE Select NP_005548.2:p.Gly37=