Canonical Allele Identifier: CA2260099868
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612598T= , CM000679.2:g.41612598T= GRCh38
NC_000017.10:g.39768850T= , CM000679.1:g.39768850T= GRCh37
NC_000017.9:g.37022376T= NCBI36
NG_008301.1:g.5230A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.91A= MANE Select ENSP00000301653.3:p.Ile31=
ENST00000301653.8:c.91A= ENSP00000301653.3:p.Ile31=
ENST00000588319.1:n.168A=
ENST00000590990.1:c.91A= ENSP00000467105.1:p.Ile31=
ENST00000593067.1:c.-313+192A= ENSP00000467124.1:n.-313+192A=
NM_005557.3:c.91A= NP_005548.2:p.Ile31=
NM_005557.4:c.91A= MANE Select NP_005548.2:p.Ile31=
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