Canonical Allele Identifier: CA2260105224
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1908627685
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41623783G>A , CM000679.2:g.41623783G>A GRCh38
NC_000017.10:g.39780035G>A , CM000679.1:g.39780035G>A GRCh37
NC_000017.9:g.37033561G>A NCBI36
NG_008625.1:g.5848C>T
NG_009090.2:g.167930C>T , LRG_401:g.167930C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.432+295C>T MANE Select ENSP00000308452.8:n.432+295C>T
ENST00000311208.12:c.432+295C>T ENSP00000308452.8:n.432+295C>T
ENST00000463128.5:c.-184+295C>T ENSP00000468672.1:n.-184+295C>T
ENST00000491673.1:n.498+295C>T
ENST00000493253.5:n.219+295C>T
ENST00000540235.5:c.183+295C>T ENSP00000441751.2:n.183+295C>T
ENST00000577817.3:c.387+295C>T ENSP00000467418.1:n.387+295C>T
NM_000422.2:c.432+295C>T NP_000413.1:n.432+295C>T
NM_000422.3:c.432+295C>T MANE Select NP_000413.1:n.432+295C>T
Search 100 bp 5'
Search 100 bp 3'