Canonical Allele Identifier: CA2260105679
Gene: KRT17 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624561G= , CM000679.2:g.41624561G= GRCh38
NC_000017.10:g.39780813G= , CM000679.1:g.39780813G= GRCh37
NC_000017.9:g.37034339G= NCBI36
NG_008625.1:g.5070C=
NG_009090.2:g.167152C= , LRG_401:g.167152C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-52C= MANE Select ENSP00000308452.8:n.-52C=
ENST00000311208.12:c.-52C= ENSP00000308452.8:n.-52C=
ENST00000463128.5:c.-313+182C= ENSP00000468672.1:n.-313+182C=
ENST00000491673.1:n.15C=
NM_000422.2:c.-52C= NP_000413.1:n.-52C=
NM_000422.3:c.-52C= MANE Select NP_000413.1:n.-52C=
Search 100 bp 5'
Search 100 bp 3'