Canonical Allele Identifier: CA500206693
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1908654063
MyVariant Identifiers: chr17:g.39780615G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624363G>T , CM000679.2:g.41624363G>T GRCh38
NC_000017.10:g.39780615G>T , CM000679.1:g.39780615G>T GRCh37
NC_000017.9:g.37034141G>T NCBI36
NG_008625.1:g.5268C>A
NG_009090.2:g.167350C>A , LRG_401:g.167350C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.147C>A MANE Select ENSP00000308452.8:p.Gly49=
ENST00000311208.12:c.147C>A ENSP00000308452.8:p.Gly49=
ENST00000463128.5:c.-312-157C>A ENSP00000468672.1:n.-312-157C>A
ENST00000491673.1:n.213C>A
ENST00000540235.5:c.-59C>A ENSP00000441751.2:n.-59C>A
ENST00000577817.3:c.102C>A ENSP00000467418.1:p.Gly34=
NM_000422.2:c.147C>A NP_000413.1:p.Gly49=
NM_000422.3:c.147C>A MANE Select NP_000413.1:p.Gly49=
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Search 100 bp 3'