Canonical Allele Identifier: CA399513074
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624324-G-T
MyVariant Identifiers: chr17:g.39780576G>T (hg19) chr17:g.41624324G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624324G>T , CM000679.2:g.41624324G>T GRCh38
NC_000017.10:g.39780576G>T , CM000679.1:g.39780576G>T GRCh37
NC_000017.9:g.37034102G>T NCBI36
NG_008625.1:g.5307C>A
NG_009090.2:g.167389C>A , LRG_401:g.167389C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.186C>A MANE Select ENSP00000308452.8:p.Ser62Arg
ENST00000311208.12:c.186C>A ENSP00000308452.8:p.Ser62Arg
ENST00000463128.5:c.-312-118C>A ENSP00000468672.1:n.-312-118C>A
ENST00000491673.1:n.252C>A
ENST00000540235.5:c.-20C>A ENSP00000441751.2:n.-20C>A
ENST00000577817.3:c.141C>A ENSP00000467418.1:p.Ser47Arg
NM_000422.2:c.186C>A NP_000413.1:p.Ser62Arg
NM_000422.3:c.186C>A MANE Select NP_000413.1:p.Ser62Arg
Search 100 bp 5'
Search 100 bp 3'