Canonical Allele Identifier: CA399513900
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780722T>G (hg19) chr17:g.41624470T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624470T>G , CM000679.2:g.41624470T>G GRCh38
NC_000017.10:g.39780722T>G , CM000679.1:g.39780722T>G GRCh37
NC_000017.9:g.37034248T>G NCBI36
NG_008625.1:g.5161A>C
NG_009090.2:g.167243A>C , LRG_401:g.167243A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.40A>C MANE Select ENSP00000308452.8:p.Ile14Leu
ENST00000311208.12:c.40A>C ENSP00000308452.8:p.Ile14Leu
ENST00000463128.5:c.-312-264A>C ENSP00000468672.1:n.-312-264A>C
ENST00000491673.1:n.106A>C
ENST00000540235.5:c.-166A>C ENSP00000441751.2:n.-166A>C
NM_000422.2:c.40A>C NP_000413.1:p.Ile14Leu
NM_000422.3:c.40A>C MANE Select NP_000413.1:p.Ile14Leu
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