Canonical Allele Identifier: CA488181136
Gene: RTL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.101349002G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882665G>A , CM000676.2:g.100882665G>A GRCh38
NC_000014.8:g.101349002G>A , CM000676.1:g.101349002G>A GRCh37
NC_000014.7:g.100418755G>A NCBI36
NG_045001.1:g.7183C>T
NG_045000.5:g.51397G>A
NG_045000.6:g.51397G>A
NG_045001.2:g.26058C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2124C>T MANE Select ENSP00000497482.1:p.Asp708=
ENST00000534062.1:c.2124C>T ENSP00000435342.1:p.Asp708=
NM_001134888.2:c.2124C>T NP_001128360.1:p.Asp708=
NM_001134888.3:c.2124C>T MANE Select NP_001128360.1:p.Asp708=