Canonical Allele Identifier: CA390994774

Gene: RTL1

Linked Data

• dbSNP Id: rs1409692677
• MyVariant Identifiers: chr14:g.101349061C>A (hg19) ; chr14:g.100882724C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.100882724C>A , CM000676.2:g.100882724C>A	GRCh38
NC_000014.8:g.101349061C>A , CM000676.1:g.101349061C>A	GRCh37
NC_000014.7:g.100418814C>A	NCBI36
NG_045001.1:g.7124G>T
NG_045000.5:g.51456C>A
NG_045000.6:g.51456C>A
NG_045001.2:g.25999G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649591.1:c.2065G>T MANE Select	ENSP00000497482.1:p.Ala689Ser
ENST00000534062.1:c.2065G>T	ENSP00000435342.1:p.Ala689Ser
NM_001134888.2:c.2065G>T	NP_001128360.1:p.Ala689Ser
NM_001134888.3:c.2065G>T MANE Select	NP_001128360.1:p.Ala689Ser