Canonical Allele Identifier: CA8563895
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs11553457
ExAC: 17:39780767 C / T
gnomAD v2: 17-39780767-C-T
gnomAD v3: 17-41624515-C-T
gnomAD v4: 17-41624515-C-T
MyVariant Identifiers: chr17:g.39780767C>T (hg19) chr17:g.41624515C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624515C>T , CM000679.2:g.41624515C>T GRCh38
NC_000017.10:g.39780767C>T , CM000679.1:g.39780767C>T GRCh37
NC_000017.9:g.37034293C>T NCBI36
NG_008625.1:g.5116G>A
NG_009090.2:g.167198G>A , LRG_401:g.167198G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-6G>A MANE Select ENSP00000308452.8:n.-6G>A
ENST00000311208.12:c.-6G>A ENSP00000308452.8:n.-6G>A
ENST00000463128.5:c.-313+228G>A ENSP00000468672.1:n.-313+228G>A
ENST00000491673.1:n.61G>A
ENST00000540235.5:c.-211G>A ENSP00000441751.2:n.-211G>A
NM_000422.2:c.-6G>A NP_000413.1:n.-6G>A
NM_000422.3:c.-6G>A MANE Select NP_000413.1:n.-6G>A
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