Canonical Allele Identifier: CA2260105657
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1908666142
gnomAD v4: 17-41624533-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624533A>T , CM000679.2:g.41624533A>T GRCh38
NC_000017.10:g.39780785A>T , CM000679.1:g.39780785A>T GRCh37
NC_000017.9:g.37034311A>T NCBI36
NG_008625.1:g.5098T>A
NG_009090.2:g.167180T>A , LRG_401:g.167180T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-24T>A MANE Select ENSP00000308452.8:n.-24T>A
ENST00000311208.12:c.-24T>A ENSP00000308452.8:n.-24T>A
ENST00000463128.5:c.-313+210T>A ENSP00000468672.1:n.-313+210T>A
ENST00000491673.1:n.43T>A
ENST00000540235.5:c.-229T>A ENSP00000441751.2:n.-229T>A
NM_000422.2:c.-24T>A NP_000413.1:n.-24T>A
NM_000422.3:c.-24T>A MANE Select NP_000413.1:n.-24T>A
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