Canonical Allele Identifier: CA399496341
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs377057928
gnomAD v4: 17-41612551-G-C
MyVariant Identifiers: chr17:g.39768803G>C (hg19) chr17:g.41612551G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612551G>C , CM000679.2:g.41612551G>C GRCh38
NC_000017.10:g.39768803G>C , CM000679.1:g.39768803G>C GRCh37
NC_000017.9:g.37022329G>C NCBI36
NG_008301.1:g.5277C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.138C>G MANE Select ENSP00000301653.3:p.Tyr46Ter
ENST00000301653.8:c.138C>G ENSP00000301653.3:p.Tyr46Ter
ENST00000588319.1:n.215C>G
ENST00000590990.1:c.138C>G ENSP00000467105.1:p.Tyr46Ter
ENST00000593067.1:c.-313+239C>G ENSP00000467124.1:n.-313+239C>G
NM_005557.3:c.138C>G NP_005548.2:p.Tyr46Ter
NM_005557.4:c.138C>G MANE Select NP_005548.2:p.Tyr46Ter
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