Canonical Allele Identifier: CA290686472
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs536728193
gnomAD v2: 17-39780823-T-A
gnomAD v3: 17-41624571-T-A
gnomAD v4: 17-41624571-T-A
MyVariant Identifiers: chr17:g.39780823T>A (hg19) chr17:g.41624571T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624571T>A , CM000679.2:g.41624571T>A GRCh38
NC_000017.10:g.39780823T>A , CM000679.1:g.39780823T>A GRCh37
NC_000017.9:g.37034349T>A NCBI36
NG_008625.1:g.5060A>T
NG_009090.2:g.167142A>T , LRG_401:g.167142A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-62A>T MANE Select ENSP00000308452.8:n.-62A>T
ENST00000311208.12:c.-62A>T ENSP00000308452.8:n.-62A>T
ENST00000463128.5:c.-313+172A>T ENSP00000468672.1:n.-313+172A>T
ENST00000491673.1:n.5A>T
NM_000422.2:c.-62A>T NP_000413.1:n.-62A>T
NM_000422.3:c.-62A>T MANE Select NP_000413.1:n.-62A>T
Search 100 bp 5'
Search 100 bp 3'