Canonical Allele Identifier: CA402583716

Gene: RAX

Linked Data

• MyVariant Identifiers: chr18:g.56936319G>T (hg19) ; chr18:g.59269087G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59269087G>T , CM000680.2:g.59269087G>T	GRCh38
NC_000018.9:g.56936319G>T , CM000680.1:g.56936319G>T	GRCh37
NC_000018.8:g.55087299G>T	NCBI36
NG_013031.1:g.9307C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334889.4:c.958C>A MANE Select	ENSP00000334813.3:p.Pro320Thr
ENST00000256852.7:c.*389C>A	ENSP00000256852.7:n.*389C>A
ENST00000334889.3:c.958C>A	ENSP00000334813.3:p.Pro320Thr
NM_013435.2:c.958C>A	NP_038463.2:p.Pro320Thr
NM_013435.3:c.958C>A MANE Select	NP_038463.2:p.Pro320Thr