Canonical Allele Identifier: CA2260105291
Gene: KRT17 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41623906G= , CM000679.2:g.41623906G= GRCh38
NC_000017.10:g.39780158G= , CM000679.1:g.39780158G= GRCh37
NC_000017.9:g.37033684G= NCBI36
NG_008625.1:g.5725C=
NG_009090.2:g.167807C= , LRG_401:g.167807C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.432+172C= MANE Select ENSP00000308452.8:n.432+172C=
ENST00000311208.12:c.432+172C= ENSP00000308452.8:n.432+172C=
ENST00000463128.5:c.-184+172C= ENSP00000468672.1:n.-184+172C=
ENST00000491673.1:n.498+172C=
ENST00000493253.5:n.219+172C=
ENST00000540235.5:c.183+172C= ENSP00000441751.2:n.183+172C=
ENST00000577817.3:c.387+172C= ENSP00000467418.1:n.387+172C=
NM_000422.2:c.432+172C= NP_000413.1:n.432+172C=
NM_000422.3:c.432+172C= MANE Select NP_000413.1:n.432+172C=
Search 100 bp 5'
Search 100 bp 3'