Canonical Allele Identifier: CA399514012
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624502-G-C
MyVariant Identifiers: chr17:g.39780754G>C (hg19) chr17:g.41624502G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624502G>C , CM000679.2:g.41624502G>C GRCh38
NC_000017.10:g.39780754G>C , CM000679.1:g.39780754G>C GRCh37
NC_000017.9:g.37034280G>C NCBI36
NG_008625.1:g.5129C>G
NG_009090.2:g.167211C>G , LRG_401:g.167211C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.8C>G MANE Select ENSP00000308452.8:p.Thr3Ser
ENST00000311208.12:c.8C>G ENSP00000308452.8:p.Thr3Ser
ENST00000463128.5:c.-313+241C>G ENSP00000468672.1:n.-313+241C>G
ENST00000491673.1:n.74C>G
ENST00000540235.5:c.-198C>G ENSP00000441751.2:n.-198C>G
NM_000422.2:c.8C>G NP_000413.1:p.Thr3Ser
NM_000422.3:c.8C>G MANE Select NP_000413.1:p.Thr3Ser
Search 100 bp 5'
Search 100 bp 3'