Canonical Allele Identifier: CA8563801
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs371268852
ExAC: 17:39780486 A / G
gnomAD v2: 17-39780486-A-G
gnomAD v3: 17-41624234-A-G
gnomAD v4: 17-41624234-A-G
MyVariant Identifiers: chr17:g.39780486A>G (hg19) chr17:g.41624234A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624234A>G , CM000679.2:g.41624234A>G GRCh38
NC_000017.10:g.39780486A>G , CM000679.1:g.39780486A>G GRCh37
NC_000017.9:g.37034012A>G NCBI36
NG_008625.1:g.5397T>C
NG_009090.2:g.167479T>C , LRG_401:g.167479T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.276T>C MANE Select ENSP00000308452.8:p.Asn92=
ENST00000311208.12:c.276T>C ENSP00000308452.8:p.Asn92=
ENST00000463128.5:c.-312-28T>C ENSP00000468672.1:n.-312-28T>C
ENST00000491673.1:n.342T>C
ENST00000493253.5:n.63T>C
ENST00000540235.5:c.71T>C ENSP00000441751.2:p.Met24Thr
ENST00000577817.3:c.231T>C ENSP00000467418.1:p.Asn77=
NM_000422.2:c.276T>C NP_000413.1:p.Asn92=
NM_000422.3:c.276T>C MANE Select NP_000413.1:p.Asn92=
Search 100 bp 5'
Search 100 bp 3'