Canonical Allele Identifier: CA399512823
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs760378776

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624286C>A , CM000679.2:g.41624286C>A GRCh38
NC_000017.10:g.39780538C>A , CM000679.1:g.39780538C>A GRCh37
NC_000017.9:g.37034064C>A NCBI36
NG_008625.1:g.5345G>T
NG_009090.2:g.167427G>T , LRG_401:g.167427G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.224G>T MANE Select ENSP00000308452.8:p.Gly75Val
ENST00000311208.12:c.224G>T ENSP00000308452.8:p.Gly75Val
ENST00000463128.5:c.-312-80G>T ENSP00000468672.1:n.-312-80G>T
ENST00000491673.1:n.290G>T
ENST00000493253.5:n.11G>T
ENST00000540235.5:c.19G>T ENSP00000441751.2:p.Val7Leu
ENST00000577817.3:c.179G>T ENSP00000467418.1:p.Gly60Val
NM_000422.2:c.224G>T NP_000413.1:p.Gly75Val
NM_000422.3:c.224G>T MANE Select NP_000413.1:p.Gly75Val