Canonical Allele Identifier: CA488181357

Gene: RTL1

Linked Data

• MyVariant Identifiers: chr14:g.101349083G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.100882746G>C , CM000676.2:g.100882746G>C	GRCh38
NC_000014.8:g.101349083G>C , CM000676.1:g.101349083G>C	GRCh37
NC_000014.7:g.100418836G>C	NCBI36
NG_045001.1:g.7102C>G
NG_045000.5:g.51478G>C
NG_045000.6:g.51478G>C
NG_045001.2:g.25977C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649591.1:c.2043C>G MANE Select	ENSP00000497482.1:p.Arg681=
ENST00000534062.1:c.2043C>G	ENSP00000435342.1:p.Arg681=
NM_001134888.2:c.2043C>G	NP_001128360.1:p.Arg681=
NM_001134888.3:c.2043C>G MANE Select	NP_001128360.1:p.Arg681=