Canonical Allele Identifier: CA8563875
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs558623005
ExAC: 17:39780707 C / G
gnomAD v2: 17-39780707-C-G
gnomAD v3: 17-41624455-C-G
gnomAD v4: 17-41624455-C-G
MyVariant Identifiers: chr17:g.39780707C>G (hg19) chr17:g.41624455C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624455C>G , CM000679.2:g.41624455C>G GRCh38
NC_000017.10:g.39780707C>G , CM000679.1:g.39780707C>G GRCh37
NC_000017.9:g.37034233C>G NCBI36
NG_008625.1:g.5176G>C
NG_009090.2:g.167258G>C , LRG_401:g.167258G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.55G>C MANE Select ENSP00000308452.8:p.Gly19Arg
ENST00000311208.12:c.55G>C ENSP00000308452.8:p.Gly19Arg
ENST00000463128.5:c.-312-249G>C ENSP00000468672.1:n.-312-249G>C
ENST00000491673.1:n.121G>C
ENST00000540235.5:c.-151G>C ENSP00000441751.2:n.-151G>C
ENST00000577817.3:c.10G>C ENSP00000467418.1:p.Gly4Arg
NM_000422.2:c.55G>C NP_000413.1:p.Gly19Arg
NM_000422.3:c.55G>C MANE Select NP_000413.1:p.Gly19Arg
Search 100 bp 5'
Search 100 bp 3'