Canonical Allele Identifier: CA399512525
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624239G>C , CM000679.2:g.41624239G>C GRCh38
NC_000017.10:g.39780491G>C , CM000679.1:g.39780491G>C GRCh37
NC_000017.9:g.37034017G>C NCBI36
NG_008625.1:g.5392C>G
NG_009090.2:g.167474C>G , LRG_401:g.167474C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.271C>G MANE Select ENSP00000308452.8:p.Leu91Val
ENST00000311208.12:c.271C>G ENSP00000308452.8:p.Leu91Val
ENST00000463128.5:c.-312-33C>G ENSP00000468672.1:n.-312-33C>G
ENST00000491673.1:n.337C>G
ENST00000493253.5:n.58C>G
ENST00000540235.5:c.66C>G ENSP00000441751.2:p.Thr22=
ENST00000577817.3:c.226C>G ENSP00000467418.1:p.Leu76Val
NM_000422.2:c.271C>G NP_000413.1:p.Leu91Val
NM_000422.3:c.271C>G MANE Select NP_000413.1:p.Leu91Val