Canonical Allele Identifier: CA626018605
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs751685332
gnomAD v2: 17-39780770-C-A
gnomAD v4: 17-41624518-C-A
MyVariant Identifiers: chr17:g.39780770C>A (hg19) chr17:g.41624518C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624518C>A , CM000679.2:g.41624518C>A GRCh38
NC_000017.10:g.39780770C>A , CM000679.1:g.39780770C>A GRCh37
NC_000017.9:g.37034296C>A NCBI36
NG_008625.1:g.5113G>T
NG_009090.2:g.167195G>T , LRG_401:g.167195G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-9G>T MANE Select ENSP00000308452.8:n.-9G>T
ENST00000311208.12:c.-9G>T ENSP00000308452.8:n.-9G>T
ENST00000463128.5:c.-313+225G>T ENSP00000468672.1:n.-313+225G>T
ENST00000491673.1:n.58G>T
ENST00000540235.5:c.-214G>T ENSP00000441751.2:n.-214G>T
NM_000422.2:c.-9G>T NP_000413.1:n.-9G>T
NM_000422.3:c.-9G>T MANE Select NP_000413.1:n.-9G>T
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