Canonical Allele Identifier: CA399512328
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624202C>A , CM000679.2:g.41624202C>A GRCh38
NC_000017.10:g.39780454C>A , CM000679.1:g.39780454C>A GRCh37
NC_000017.9:g.37033980C>A NCBI36
NG_008625.1:g.5429G>T
NG_009090.2:g.167511G>T , LRG_401:g.167511G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.308G>T MANE Select ENSP00000308452.8:p.Arg103Leu
ENST00000311208.12:c.308G>T ENSP00000308452.8:p.Arg103Leu
ENST00000463128.5:c.-308G>T ENSP00000468672.1:n.-308G>T
ENST00000491673.1:n.374G>T
ENST00000493253.5:n.95G>T
ENST00000540235.5:c.72-11G>T ENSP00000441751.2:n.72-11G>T
ENST00000577817.3:c.263G>T ENSP00000467418.1:p.Arg88Leu
NM_000422.2:c.308G>T NP_000413.1:p.Arg103Leu
NM_000422.3:c.308G>T MANE Select NP_000413.1:p.Arg103Leu