Canonical Allele Identifier: CA399513560
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624401-C-T
MyVariant Identifiers: chr17:g.39780653C>T (hg19) chr17:g.41624401C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624401C>T , CM000679.2:g.41624401C>T GRCh38
NC_000017.10:g.39780653C>T , CM000679.1:g.39780653C>T GRCh37
NC_000017.9:g.37034179C>T NCBI36
NG_008625.1:g.5230G>A
NG_009090.2:g.167312G>A , LRG_401:g.167312G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.109G>A MANE Select ENSP00000308452.8:p.Ala37Thr
ENST00000311208.12:c.109G>A ENSP00000308452.8:p.Ala37Thr
ENST00000463128.5:c.-312-195G>A ENSP00000468672.1:n.-312-195G>A
ENST00000491673.1:n.175G>A
ENST00000540235.5:c.-97G>A ENSP00000441751.2:n.-97G>A
ENST00000577817.3:c.64G>A ENSP00000467418.1:p.Ala22Thr
NM_000422.2:c.109G>A NP_000413.1:p.Ala37Thr
NM_000422.3:c.109G>A MANE Select NP_000413.1:p.Ala37Thr
Search 100 bp 5'
Search 100 bp 3'