Canonical Allele Identifier: CA2260099928
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612697G= , CM000679.2:g.41612697G= GRCh38
NC_000017.10:g.39768949G= , CM000679.1:g.39768949G= GRCh37
NC_000017.9:g.37022475G= NCBI36
NG_008301.1:g.5131C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-9C= MANE Select ENSP00000301653.3:n.-9C=
ENST00000301653.8:c.-9C= ENSP00000301653.3:n.-9C=
ENST00000588319.1:n.69C=
ENST00000590990.1:c.-9C= ENSP00000467105.1:n.-9C=
ENST00000593067.1:c.-313+93C= ENSP00000467124.1:n.-313+93C=
NM_005557.3:c.-9C= NP_005548.2:n.-9C=
NM_005557.4:c.-9C= MANE Select NP_005548.2:n.-9C=
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