Canonical Allele Identifier: CA402583545

Gene: RAX

Linked Data

• MyVariant Identifiers: chr18:g.56936277C>T (hg19) ; chr18:g.59269045C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59269045C>T , CM000680.2:g.59269045C>T	GRCh38
NC_000018.9:g.56936277C>T , CM000680.1:g.56936277C>T	GRCh37
NC_000018.8:g.55087257C>T	NCBI36
NG_013031.1:g.9349G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334889.4:c.1000G>A MANE Select	ENSP00000334813.3:p.Glu334Lys
ENST00000256852.7:c.*431G>A	ENSP00000256852.7:n.*431G>A
ENST00000334889.3:c.1000G>A	ENSP00000334813.3:p.Glu334Lys
NM_013435.2:c.1000G>A	NP_038463.2:p.Glu334Lys
NM_013435.3:c.1000G>A MANE Select	NP_038463.2:p.Glu334Lys