Canonical Allele Identifier: CA8563772
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs374327168

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624125G>C , CM000679.2:g.41624125G>C GRCh38
NC_000017.10:g.39780377G>C , CM000679.1:g.39780377G>C GRCh37
NC_000017.9:g.37033903G>C NCBI36
NG_008625.1:g.5506C>G
NG_009090.2:g.167588C>G , LRG_401:g.167588C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.385C>G MANE Select ENSP00000308452.8:p.Arg129Gly
ENST00000311208.12:c.385C>G ENSP00000308452.8:p.Arg129Gly
ENST00000463128.5:c.-231C>G ENSP00000468672.1:n.-231C>G
ENST00000491673.1:n.451C>G
ENST00000493253.5:n.172C>G
ENST00000540235.5:c.136C>G ENSP00000441751.2:p.Arg46Gly
ENST00000577817.3:c.340C>G ENSP00000467418.1:p.Arg114Gly
NM_000422.2:c.385C>G NP_000413.1:p.Arg129Gly
NM_000422.3:c.385C>G MANE Select NP_000413.1:p.Arg129Gly