Canonical Allele Identifier: CA390996572

Gene: RTL1

Linked Data

• MyVariant Identifiers: chr14:g.101349863G>T (hg19) ; chr14:g.100883526G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.100883526G>T , CM000676.2:g.100883526G>T	GRCh38
NC_000014.8:g.101349863G>T , CM000676.1:g.101349863G>T	GRCh37
NC_000014.7:g.100419616G>T	NCBI36
NG_045001.1:g.6322C>A
NG_045000.5:g.52258G>T
NG_045000.6:g.52258G>T
NG_045001.2:g.25197C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649591.1:c.1263C>A MANE Select	ENSP00000497482.1:p.His421Gln
ENST00000534062.1:c.1263C>A	ENSP00000435342.1:p.His421Gln
NM_001134888.2:c.1263C>A	NP_001128360.1:p.His421Gln
NM_001134888.3:c.1263C>A MANE Select	NP_001128360.1:p.His421Gln