Canonical Allele Identifier: CA216624
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14599
dbSNP Id: rs59977263

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624206C>T , CM000679.2:g.41624206C>T GRCh38
NC_000017.10:g.39780458C>T , CM000679.1:g.39780458C>T GRCh37
NC_000017.9:g.37033984C>T NCBI36
NG_008625.1:g.5425G>A
NG_009090.2:g.167507G>A , LRG_401:g.167507G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.304G>A MANE Select ENSP00000308452.8:p.Val102Met
ENST00000311208.12:c.304G>A ENSP00000308452.8:p.Val102Met
ENST00000463128.5:c.-312G>A ENSP00000468672.1:n.-312G>A
ENST00000491673.1:n.370G>A
ENST00000493253.5:n.91G>A
ENST00000540235.5:c.72-15G>A ENSP00000441751.2:n.72-15G>A
ENST00000577817.3:c.259G>A ENSP00000467418.1:p.Val87Met
NM_000422.2:c.304G>A NP_000413.1:p.Val102Met
NM_000422.3:c.304G>A MANE Select NP_000413.1:p.Val102Met