Canonical Allele Identifier: CA402583777

Gene: RAX

Linked Data

• MyVariant Identifiers: chr18:g.56936331C>A (hg19) ; chr18:g.59269099C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59269099C>A , CM000680.2:g.59269099C>A	GRCh38
NC_000018.9:g.56936331C>A , CM000680.1:g.56936331C>A	GRCh37
NC_000018.8:g.55087311C>A	NCBI36
NG_013031.1:g.9295G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334889.4:c.946G>T MANE Select	ENSP00000334813.3:p.Asp316Tyr
ENST00000256852.7:c.*377G>T	ENSP00000256852.7:n.*377G>T
ENST00000334889.3:c.946G>T	ENSP00000334813.3:p.Asp316Tyr
NM_013435.2:c.946G>T	NP_038463.2:p.Asp316Tyr
NM_013435.3:c.946G>T MANE Select	NP_038463.2:p.Asp316Tyr