Canonical Allele Identifier: CA8563834
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs201047424
ExAC: 17:39780611 T / A
gnomAD v2: 17-39780611-T-A
gnomAD v3: 17-41624359-T-A
gnomAD v4: 17-41624359-T-A
MyVariant Identifiers: chr17:g.39780611T>A (hg19) chr17:g.41624359T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624359T>A , CM000679.2:g.41624359T>A GRCh38
NC_000017.10:g.39780611T>A , CM000679.1:g.39780611T>A GRCh37
NC_000017.9:g.37034137T>A NCBI36
NG_008625.1:g.5272A>T
NG_009090.2:g.167354A>T , LRG_401:g.167354A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.151A>T MANE Select ENSP00000308452.8:p.Thr51Ser
ENST00000311208.12:c.151A>T ENSP00000308452.8:p.Thr51Ser
ENST00000463128.5:c.-312-153A>T ENSP00000468672.1:n.-312-153A>T
ENST00000491673.1:n.217A>T
ENST00000540235.5:c.-55A>T ENSP00000441751.2:n.-55A>T
ENST00000577817.3:c.106A>T ENSP00000467418.1:p.Thr36Ser
NM_000422.2:c.151A>T NP_000413.1:p.Thr51Ser
NM_000422.3:c.151A>T MANE Select NP_000413.1:p.Thr51Ser
Search 100 bp 5'
Search 100 bp 3'