Canonical Allele Identifier: CA2260099956
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612736A= , CM000679.2:g.41612736A= GRCh38
NC_000017.10:g.39768988A= , CM000679.1:g.39768988A= GRCh37
NC_000017.9:g.37022514A= NCBI36
NG_008301.1:g.5092T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-48T= MANE Select ENSP00000301653.3:n.-48T=
ENST00000301653.8:c.-48T= ENSP00000301653.3:n.-48T=
ENST00000588319.1:n.30T=
ENST00000590990.1:c.-36-12T= ENSP00000467105.1:n.-36-12T=
ENST00000593067.1:c.-313+54T= ENSP00000467124.1:n.-313+54T=
NM_005557.3:c.-48T= NP_005548.2:n.-48T=
NM_005557.4:c.-48T= MANE Select NP_005548.2:n.-48T=
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