Canonical Allele Identifier: CA399512921
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624301C>G , CM000679.2:g.41624301C>G GRCh38
NC_000017.10:g.39780553C>G , CM000679.1:g.39780553C>G GRCh37
NC_000017.9:g.37034079C>G NCBI36
NG_008625.1:g.5330G>C
NG_009090.2:g.167412G>C , LRG_401:g.167412G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.209G>C MANE Select ENSP00000308452.8:p.Gly70Ala
ENST00000311208.12:c.209G>C ENSP00000308452.8:p.Gly70Ala
ENST00000463128.5:c.-312-95G>C ENSP00000468672.1:n.-312-95G>C
ENST00000491673.1:n.275G>C
ENST00000540235.5:c.4G>C ENSP00000441751.2:p.Ala2Pro
ENST00000577817.3:c.164G>C ENSP00000467418.1:p.Gly55Ala
NM_000422.2:c.209G>C NP_000413.1:p.Gly70Ala
NM_000422.3:c.209G>C MANE Select NP_000413.1:p.Gly70Ala