Canonical Allele Identifier: CA399513077
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1190242046

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624325C>A , CM000679.2:g.41624325C>A GRCh38
NC_000017.10:g.39780577C>A , CM000679.1:g.39780577C>A GRCh37
NC_000017.9:g.37034103C>A NCBI36
NG_008625.1:g.5306G>T
NG_009090.2:g.167388G>T , LRG_401:g.167388G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.185G>T MANE Select ENSP00000308452.8:p.Ser62Ile
ENST00000311208.12:c.185G>T ENSP00000308452.8:p.Ser62Ile
ENST00000463128.5:c.-312-119G>T ENSP00000468672.1:n.-312-119G>T
ENST00000491673.1:n.251G>T
ENST00000540235.5:c.-21G>T ENSP00000441751.2:n.-21G>T
ENST00000577817.3:c.140G>T ENSP00000467418.1:p.Ser47Ile
NM_000422.2:c.185G>T NP_000413.1:p.Ser62Ile
NM_000422.3:c.185G>T MANE Select NP_000413.1:p.Ser62Ile