Canonical Allele Identifier: CA399511703
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624114G>T , CM000679.2:g.41624114G>T GRCh38
NC_000017.10:g.39780366G>T , CM000679.1:g.39780366G>T GRCh37
NC_000017.9:g.37033892G>T NCBI36
NG_008625.1:g.5517C>A
NG_009090.2:g.167599C>A , LRG_401:g.167599C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.396C>A MANE Select ENSP00000308452.8:p.Ser132Arg
ENST00000311208.12:c.396C>A ENSP00000308452.8:p.Ser132Arg
ENST00000463128.5:c.-220C>A ENSP00000468672.1:n.-220C>A
ENST00000491673.1:n.462C>A
ENST00000493253.5:n.183C>A
ENST00000540235.5:c.147C>A ENSP00000441751.2:p.Ser49Arg
ENST00000577817.3:c.351C>A ENSP00000467418.1:p.Ser117Arg
NM_000422.2:c.396C>A NP_000413.1:p.Ser132Arg
NM_000422.3:c.396C>A MANE Select NP_000413.1:p.Ser132Arg