Canonical Allele Identifier: CA390994796

Gene: RTL1

Linked Data

• COSMIC: COSM5604749
• MyVariant Identifiers: chr14:g.101349069C>T (hg19) ; chr14:g.100882732C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.100882732C>T , CM000676.2:g.100882732C>T	GRCh38
NC_000014.8:g.101349069C>T , CM000676.1:g.101349069C>T	GRCh37
NC_000014.7:g.100418822C>T	NCBI36
NG_045001.1:g.7116G>A
NG_045000.5:g.51464C>T
NG_045000.6:g.51464C>T
NG_045001.2:g.25991G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649591.1:c.2057G>A MANE Select	ENSP00000497482.1:p.Trp686Ter
ENST00000534062.1:c.2057G>A	ENSP00000435342.1:p.Trp686Ter
NM_001134888.2:c.2057G>A	NP_001128360.1:p.Trp686Ter
NM_001134888.3:c.2057G>A MANE Select	NP_001128360.1:p.Trp686Ter