Canonical Allele Identifier: CA500206611
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780561A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624309A>C , CM000679.2:g.41624309A>C GRCh38
NC_000017.10:g.39780561A>C , CM000679.1:g.39780561A>C GRCh37
NC_000017.9:g.37034087A>C NCBI36
NG_008625.1:g.5322T>G
NG_009090.2:g.167404T>G , LRG_401:g.167404T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.201T>G MANE Select ENSP00000308452.8:p.Gly67=
ENST00000311208.12:c.201T>G ENSP00000308452.8:p.Gly67=
ENST00000463128.5:c.-312-103T>G ENSP00000468672.1:n.-312-103T>G
ENST00000491673.1:n.267T>G
ENST00000540235.5:c.-5T>G ENSP00000441751.2:n.-5T>G
ENST00000577817.3:c.156T>G ENSP00000467418.1:p.Gly52=
NM_000422.2:c.201T>G NP_000413.1:p.Gly67=
NM_000422.3:c.201T>G MANE Select NP_000413.1:p.Gly67=
Search 100 bp 5'
Search 100 bp 3'