Canonical Allele Identifier: CA399496102
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908242150
MyVariant Identifiers: chr17:g.39768771G>C (hg19) chr17:g.41612519G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612519G>C , CM000679.2:g.41612519G>C GRCh38
NC_000017.10:g.39768771G>C , CM000679.1:g.39768771G>C GRCh37
NC_000017.9:g.37022297G>C NCBI36
NG_008301.1:g.5309C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.170C>G MANE Select ENSP00000301653.3:p.Ser57Cys
ENST00000301653.8:c.170C>G ENSP00000301653.3:p.Ser57Cys
ENST00000588319.1:n.247C>G
ENST00000593067.1:c.-312-233C>G ENSP00000467124.1:n.-312-233C>G
NM_005557.3:c.170C>G NP_005548.2:p.Ser57Cys
NM_005557.4:c.170C>G MANE Select NP_005548.2:p.Ser57Cys
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