Canonical Allele Identifier: CA500206192
Gene: KRT17 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39780390G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624138G>C , CM000679.2:g.41624138G>C GRCh38
NC_000017.10:g.39780390G>C , CM000679.1:g.39780390G>C GRCh37
NC_000017.9:g.37033916G>C NCBI36
NG_008625.1:g.5493C>G
NG_009090.2:g.167575C>G , LRG_401:g.167575C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.372C>G MANE Select ENSP00000308452.8:p.Ala124=
ENST00000311208.12:c.372C>G ENSP00000308452.8:p.Ala124=
ENST00000463128.5:c.-244C>G ENSP00000468672.1:n.-244C>G
ENST00000491673.1:n.438C>G
ENST00000493253.5:n.159C>G
ENST00000540235.5:c.123C>G ENSP00000441751.2:p.Ala41=
ENST00000577817.3:c.327C>G ENSP00000467418.1:p.Ala109=
NM_000422.2:c.372C>G NP_000413.1:p.Ala124=
NM_000422.3:c.372C>G MANE Select NP_000413.1:p.Ala124=
Search 100 bp 5'
Search 100 bp 3'