Canonical Allele Identifier: CA390995007
Gene: RTL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.101349162T>A (hg19) chr14:g.100882825T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882825T>A , CM000676.2:g.100882825T>A GRCh38
NC_000014.8:g.101349162T>A , CM000676.1:g.101349162T>A GRCh37
NC_000014.7:g.100418915T>A NCBI36
NG_045001.1:g.7023A>T
NG_045000.5:g.51557T>A
NG_045000.6:g.51557T>A
NG_045001.2:g.25898A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1964A>T MANE Select ENSP00000497482.1:p.Asp655Val
ENST00000534062.1:c.1964A>T ENSP00000435342.1:p.Asp655Val
NM_001134888.2:c.1964A>T NP_001128360.1:p.Asp655Val
NM_001134888.3:c.1964A>T MANE Select NP_001128360.1:p.Asp655Val
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