Canonical Allele Identifier: CA2260105690
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624578G= , CM000679.2:g.41624578G= GRCh38
NC_000017.10:g.39780830G= , CM000679.1:g.39780830G= GRCh37
NC_000017.9:g.37034356G= NCBI36
NG_008625.1:g.5053C=
NG_009090.2:g.167135C= , LRG_401:g.167135C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463128.5:c.-313+165C= ENSP00000468672.1:n.-313+165C=
NM_000422.2:c.-69C= NP_000413.1:n.-69C=