Canonical Allele Identifier: CA399512478
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624231G>T , CM000679.2:g.41624231G>T GRCh38
NC_000017.10:g.39780483G>T , CM000679.1:g.39780483G>T GRCh37
NC_000017.9:g.37034009G>T NCBI36
NG_008625.1:g.5400C>A
NG_009090.2:g.167482C>A , LRG_401:g.167482C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.279C>A MANE Select ENSP00000308452.8:p.Asp93Glu
ENST00000311208.12:c.279C>A ENSP00000308452.8:p.Asp93Glu
ENST00000463128.5:c.-312-25C>A ENSP00000468672.1:n.-312-25C>A
ENST00000491673.1:n.345C>A
ENST00000493253.5:n.66C>A
ENST00000540235.5:c.71+3C>A ENSP00000441751.2:n.71+3C>A
ENST00000577817.3:c.234C>A ENSP00000467418.1:p.Asp78Glu
NM_000422.2:c.279C>A NP_000413.1:p.Asp93Glu
NM_000422.3:c.279C>A MANE Select NP_000413.1:p.Asp93Glu