Canonical Allele Identifier: CA390996172
Gene: RTL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.101349682T>C (hg19) chr14:g.100883345T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883345T>C , CM000676.2:g.100883345T>C GRCh38
NC_000014.8:g.101349682T>C , CM000676.1:g.101349682T>C GRCh37
NC_000014.7:g.100419435T>C NCBI36
NG_045001.1:g.6503A>G
NG_045000.5:g.52077T>C
NG_045000.6:g.52077T>C
NG_045001.2:g.25378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1444A>G MANE Select ENSP00000497482.1:p.Ile482Val
ENST00000534062.1:c.1444A>G ENSP00000435342.1:p.Ile482Val
NM_001134888.2:c.1444A>G NP_001128360.1:p.Ile482Val
NM_001134888.3:c.1444A>G MANE Select NP_001128360.1:p.Ile482Val
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Search 100 bp 3'