Canonical Allele Identifier: CA500012325
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs200589130
MyVariant Identifiers: chr17:g.39780708G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624456G>T , CM000679.2:g.41624456G>T GRCh38
NC_000017.10:g.39780708G>T , CM000679.1:g.39780708G>T GRCh37
NC_000017.9:g.37034234G>T NCBI36
NG_008625.1:g.5175C>A
NG_009090.2:g.167257C>A , LRG_401:g.167257C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.54C>A MANE Select ENSP00000308452.8:p.Ser18=
ENST00000311208.12:c.54C>A ENSP00000308452.8:p.Ser18=
ENST00000463128.5:c.-312-250C>A ENSP00000468672.1:n.-312-250C>A
ENST00000491673.1:n.120C>A
ENST00000540235.5:c.-152C>A ENSP00000441751.2:n.-152C>A
ENST00000577817.3:c.9C>A ENSP00000467418.1:p.Ser3=
NM_000422.2:c.54C>A NP_000413.1:p.Ser18=
NM_000422.3:c.54C>A MANE Select NP_000413.1:p.Ser18=
Search 100 bp 5'
Search 100 bp 3'