Canonical Allele Identifier: CA8563857
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs554504293
ExAC: 17:39780682 G / T
gnomAD v2: 17-39780682-G-T
gnomAD v3: 17-41624430-G-T
gnomAD v4: 17-41624430-G-T
MyVariant Identifiers: chr17:g.39780682G>T (hg19) chr17:g.41624430G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624430G>T , CM000679.2:g.41624430G>T GRCh38
NC_000017.10:g.39780682G>T , CM000679.1:g.39780682G>T GRCh37
NC_000017.9:g.37034208G>T NCBI36
NG_008625.1:g.5201C>A
NG_009090.2:g.167283C>A , LRG_401:g.167283C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.80C>A MANE Select ENSP00000308452.8:p.Thr27Asn
ENST00000311208.12:c.80C>A ENSP00000308452.8:p.Thr27Asn
ENST00000463128.5:c.-312-224C>A ENSP00000468672.1:n.-312-224C>A
ENST00000491673.1:n.146C>A
ENST00000540235.5:c.-126C>A ENSP00000441751.2:n.-126C>A
ENST00000577817.3:c.35C>A ENSP00000467418.1:p.Thr12Asn
NM_000422.2:c.80C>A NP_000413.1:p.Thr27Asn
NM_000422.3:c.80C>A MANE Select NP_000413.1:p.Thr27Asn
Search 100 bp 5'
Search 100 bp 3'