Canonical Allele Identifier: CA2260099953
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612732A= , CM000679.2:g.41612732A= GRCh38
NC_000017.10:g.39768984A= , CM000679.1:g.39768984A= GRCh37
NC_000017.9:g.37022510A= NCBI36
NG_008301.1:g.5096T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-44T= MANE Select ENSP00000301653.3:n.-44T=
ENST00000301653.8:c.-44T= ENSP00000301653.3:n.-44T=
ENST00000588319.1:n.34T=
ENST00000590990.1:c.-36-8T= ENSP00000467105.1:n.-36-8T=
ENST00000593067.1:c.-313+58T= ENSP00000467124.1:n.-313+58T=
NM_005557.3:c.-44T= NP_005548.2:n.-44T=
NM_005557.4:c.-44T= MANE Select NP_005548.2:n.-44T=
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