Canonical Allele Identifier: CA500206683
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624354-G-T
MyVariant Identifiers: chr17:g.39780606G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624354G>T , CM000679.2:g.41624354G>T GRCh38
NC_000017.10:g.39780606G>T , CM000679.1:g.39780606G>T GRCh37
NC_000017.9:g.37034132G>T NCBI36
NG_008625.1:g.5277C>A
NG_009090.2:g.167359C>A , LRG_401:g.167359C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.156C>A MANE Select ENSP00000308452.8:p.Leu52=
ENST00000311208.12:c.156C>A ENSP00000308452.8:p.Leu52=
ENST00000463128.5:c.-312-148C>A ENSP00000468672.1:n.-312-148C>A
ENST00000491673.1:n.222C>A
ENST00000540235.5:c.-50C>A ENSP00000441751.2:n.-50C>A
ENST00000577817.3:c.111C>A ENSP00000467418.1:p.Leu37=
NM_000422.2:c.156C>A NP_000413.1:p.Leu52=
NM_000422.3:c.156C>A MANE Select NP_000413.1:p.Leu52=
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