Canonical Allele Identifier: CA399496095
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908242150
gnomAD v4: 17-41612519-G-A
MyVariant Identifiers: chr17:g.39768771G>A (hg19) chr17:g.41612519G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.170C>T MANE Select ENSP00000301653.3:p.Ser57Phe
ENST00000301653.8:c.170C>T ENSP00000301653.3:p.Ser57Phe
ENST00000588319.1:n.247C>T
ENST00000593067.1:c.-312-233C>T ENSP00000467124.1:n.-312-233C>T
NM_005557.3:c.170C>T NP_005548.2:p.Ser57Phe
NM_005557.4:c.170C>T MANE Select NP_005548.2:p.Ser57Phe
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