Canonical Allele Identifier: CA399511846
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624131G>C , CM000679.2:g.41624131G>C GRCh38
NC_000017.10:g.39780383G>C , CM000679.1:g.39780383G>C GRCh37
NC_000017.9:g.37033909G>C NCBI36
NG_008625.1:g.5500C>G
NG_009090.2:g.167582C>G , LRG_401:g.167582C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.379C>G MANE Select ENSP00000308452.8:p.Pro127Ala
ENST00000311208.12:c.379C>G ENSP00000308452.8:p.Pro127Ala
ENST00000463128.5:c.-237C>G ENSP00000468672.1:n.-237C>G
ENST00000491673.1:n.445C>G
ENST00000493253.5:n.166C>G
ENST00000540235.5:c.130C>G ENSP00000441751.2:p.Pro44Ala
ENST00000577817.3:c.334C>G ENSP00000467418.1:p.Pro112Ala
NM_000422.2:c.379C>G NP_000413.1:p.Pro127Ala
NM_000422.3:c.379C>G MANE Select NP_000413.1:p.Pro127Ala