Canonical Allele Identifier: CA2637841052
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624570-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624570T>A , CM000679.2:g.41624570T>A GRCh38
NC_000017.10:g.39780822T>A , CM000679.1:g.39780822T>A GRCh37
NC_000017.9:g.37034348T>A NCBI36
NG_008625.1:g.5061A>T
NG_009090.2:g.167143A>T , LRG_401:g.167143A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-61A>T MANE Select ENSP00000308452.8:n.-61A>T
ENST00000311208.12:c.-61A>T ENSP00000308452.8:n.-61A>T
ENST00000463128.5:c.-313+173A>T ENSP00000468672.1:n.-313+173A>T
ENST00000491673.1:n.6A>T
NM_000422.2:c.-61A>T NP_000413.1:n.-61A>T
NM_000422.3:c.-61A>T MANE Select NP_000413.1:n.-61A>T
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