Canonical Allele Identifier: CA2260099866
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612594G= , CM000679.2:g.41612594G= GRCh38
NC_000017.10:g.39768846G= , CM000679.1:g.39768846G= GRCh37
NC_000017.9:g.37022372G= NCBI36
NG_008301.1:g.5234C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.95C= MANE Select ENSP00000301653.3:p.Ser32=
ENST00000301653.8:c.95C= ENSP00000301653.3:p.Ser32=
ENST00000588319.1:n.172C=
ENST00000590990.1:c.95C= ENSP00000467105.1:p.Ser32=
ENST00000593067.1:c.-313+196C= ENSP00000467124.1:n.-313+196C=
NM_005557.3:c.95C= NP_005548.2:p.Ser32=
NM_005557.4:c.95C= MANE Select NP_005548.2:p.Ser32=
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