Canonical Allele Identifier: CA8563776
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs749886161

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624129G>A , CM000679.2:g.41624129G>A GRCh38
NC_000017.10:g.39780381G>A , CM000679.1:g.39780381G>A GRCh37
NC_000017.9:g.37033907G>A NCBI36
NG_008625.1:g.5502C>T
NG_009090.2:g.167584C>T , LRG_401:g.167584C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.381C>T MANE Select ENSP00000308452.8:p.Pro127=
ENST00000311208.12:c.381C>T ENSP00000308452.8:p.Pro127=
ENST00000463128.5:c.-235C>T ENSP00000468672.1:n.-235C>T
ENST00000491673.1:n.447C>T
ENST00000493253.5:n.168C>T
ENST00000540235.5:c.132C>T ENSP00000441751.2:p.Pro44=
ENST00000577817.3:c.336C>T ENSP00000467418.1:p.Pro112=
NM_000422.2:c.381C>T NP_000413.1:p.Pro127=
NM_000422.3:c.381C>T MANE Select NP_000413.1:p.Pro127=