Canonical Allele Identifier: CA399511820
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624128C>G , CM000679.2:g.41624128C>G GRCh38
NC_000017.10:g.39780380C>G , CM000679.1:g.39780380C>G GRCh37
NC_000017.9:g.37033906C>G NCBI36
NG_008625.1:g.5503G>C
NG_009090.2:g.167585G>C , LRG_401:g.167585G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.382G>C MANE Select ENSP00000308452.8:p.Ala128Pro
ENST00000311208.12:c.382G>C ENSP00000308452.8:p.Ala128Pro
ENST00000463128.5:c.-234G>C ENSP00000468672.1:n.-234G>C
ENST00000491673.1:n.448G>C
ENST00000493253.5:n.169G>C
ENST00000540235.5:c.133G>C ENSP00000441751.2:p.Ala45Pro
ENST00000577817.3:c.337G>C ENSP00000467418.1:p.Ala113Pro
NM_000422.2:c.382G>C NP_000413.1:p.Ala128Pro
NM_000422.3:c.382G>C MANE Select NP_000413.1:p.Ala128Pro