Canonical Allele Identifier: CA626018601
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs764060766
gnomAD v2: 17-39780768-G-T
MyVariant Identifiers: chr17:g.39780768G>T (hg19) chr17:g.41624516G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624516G>T , CM000679.2:g.41624516G>T GRCh38
NC_000017.10:g.39780768G>T , CM000679.1:g.39780768G>T GRCh37
NC_000017.9:g.37034294G>T NCBI36
NG_008625.1:g.5115C>A
NG_009090.2:g.167197C>A , LRG_401:g.167197C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-7C>A MANE Select ENSP00000308452.8:n.-7C>A
ENST00000311208.12:c.-7C>A ENSP00000308452.8:n.-7C>A
ENST00000463128.5:c.-313+227C>A ENSP00000468672.1:n.-313+227C>A
ENST00000491673.1:n.60C>A
ENST00000540235.5:c.-212C>A ENSP00000441751.2:n.-212C>A
NM_000422.2:c.-7C>A NP_000413.1:n.-7C>A
NM_000422.3:c.-7C>A MANE Select NP_000413.1:n.-7C>A
Search 100 bp 5'
Search 100 bp 3'