Canonical Allele Identifier: CA390996078
Gene: RTL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.101349645A>G (hg19) chr14:g.100883308A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883308A>G , CM000676.2:g.100883308A>G GRCh38
NC_000014.8:g.101349645A>G , CM000676.1:g.101349645A>G GRCh37
NC_000014.7:g.100419398A>G NCBI36
NG_045001.1:g.6540T>C
NG_045000.5:g.52040A>G
NG_045000.6:g.52040A>G
NG_045001.2:g.25415T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1481T>C MANE Select ENSP00000497482.1:p.Ile494Thr
ENST00000534062.1:c.1481T>C ENSP00000435342.1:p.Ile494Thr
NM_001134888.2:c.1481T>C NP_001128360.1:p.Ile494Thr
NM_001134888.3:c.1481T>C MANE Select NP_001128360.1:p.Ile494Thr
Search 100 bp 5'
Search 100 bp 3'