Canonical Allele Identifier: CA500206474
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612590-G-T
MyVariant Identifiers: chr17:g.39768842G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612590G>T , CM000679.2:g.41612590G>T GRCh38
NC_000017.10:g.39768842G>T , CM000679.1:g.39768842G>T GRCh37
NC_000017.9:g.37022368G>T NCBI36
NG_008301.1:g.5238C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.99C>A MANE Select ENSP00000301653.3:p.Ser33=
ENST00000301653.8:c.99C>A ENSP00000301653.3:p.Ser33=
ENST00000588319.1:n.176C>A
ENST00000590990.1:c.99C>A ENSP00000467105.1:p.Ser33=
ENST00000593067.1:c.-313+200C>A ENSP00000467124.1:n.-313+200C>A
NM_005557.3:c.99C>A NP_005548.2:p.Ser33=
NM_005557.4:c.99C>A MANE Select NP_005548.2:p.Ser33=
Search 100 bp 5'
Search 100 bp 3'