Canonical Allele Identifier: CA399511809
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1908640933

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624127G>A , CM000679.2:g.41624127G>A GRCh38
NC_000017.10:g.39780379G>A , CM000679.1:g.39780379G>A GRCh37
NC_000017.9:g.37033905G>A NCBI36
NG_008625.1:g.5504C>T
NG_009090.2:g.167586C>T , LRG_401:g.167586C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.383C>T MANE Select ENSP00000308452.8:p.Ala128Val
ENST00000311208.12:c.383C>T ENSP00000308452.8:p.Ala128Val
ENST00000463128.5:c.-233C>T ENSP00000468672.1:n.-233C>T
ENST00000491673.1:n.449C>T
ENST00000493253.5:n.170C>T
ENST00000540235.5:c.134C>T ENSP00000441751.2:p.Ala45Val
ENST00000577817.3:c.338C>T ENSP00000467418.1:p.Ala113Val
NM_000422.2:c.383C>T NP_000413.1:p.Ala128Val
NM_000422.3:c.383C>T MANE Select NP_000413.1:p.Ala128Val