Canonical Allele Identifier: CA399511784
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624124C>A , CM000679.2:g.41624124C>A GRCh38
NC_000017.10:g.39780376C>A , CM000679.1:g.39780376C>A GRCh37
NC_000017.9:g.37033902C>A NCBI36
NG_008625.1:g.5507G>T
NG_009090.2:g.167589G>T , LRG_401:g.167589G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.386G>T MANE Select ENSP00000308452.8:p.Arg129Leu
ENST00000311208.12:c.386G>T ENSP00000308452.8:p.Arg129Leu
ENST00000463128.5:c.-230G>T ENSP00000468672.1:n.-230G>T
ENST00000491673.1:n.452G>T
ENST00000493253.5:n.173G>T
ENST00000540235.5:c.137G>T ENSP00000441751.2:p.Arg46Leu
ENST00000577817.3:c.341G>T ENSP00000467418.1:p.Arg114Leu
NM_000422.2:c.386G>T NP_000413.1:p.Arg129Leu
NM_000422.3:c.386G>T MANE Select NP_000413.1:p.Arg129Leu