Canonical Allele Identifier: CA626018611
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1409432459
gnomAD v2: 17-39780777-A-G
gnomAD v4: 17-41624525-A-G
MyVariant Identifiers: chr17:g.39780777A>G (hg19) chr17:g.41624525A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624525A>G , CM000679.2:g.41624525A>G GRCh38
NC_000017.10:g.39780777A>G , CM000679.1:g.39780777A>G GRCh37
NC_000017.9:g.37034303A>G NCBI36
NG_008625.1:g.5106T>C
NG_009090.2:g.167188T>C , LRG_401:g.167188T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-16T>C MANE Select ENSP00000308452.8:n.-16T>C
ENST00000311208.12:c.-16T>C ENSP00000308452.8:n.-16T>C
ENST00000463128.5:c.-313+218T>C ENSP00000468672.1:n.-313+218T>C
ENST00000491673.1:n.51T>C
ENST00000540235.5:c.-221T>C ENSP00000441751.2:n.-221T>C
NM_000422.2:c.-16T>C NP_000413.1:n.-16T>C
NM_000422.3:c.-16T>C MANE Select NP_000413.1:n.-16T>C
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