Canonical Allele Identifier: CA365650647

Gene: ARG1 MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131579222C>T , CM000668.2:g.131579222C>T	GRCh38
NC_000006.11:g.131900362C>T , CM000668.1:g.131900362C>T	GRCh37
NC_000006.10:g.131942055C>T	NCBI36
NG_007086.2:g.10998C>T
NG_031860.1:g.54002G>A
NG_031860.2:g.54002G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000045.4:c.242C>T (ARG1) MANE Select	NP_000036.2:p.Ala81Val
ENST00000368087.8:c.242C>T (ARG1) MANE Select	ENSP00000357066.3:p.Ala81Val
NM_000045.3:c.242C>T (ARG1)	NP_000036.2:p.Ala81Val
NM_001244438.1:c.266C>T (ARG1)	NP_001231367.1:p.Ala89Val
NM_001244438.2:c.266C>T (ARG1)	NP_001231367.1:p.Ala89Val
NM_001270521.1:c.4078-4927G>A (MED23)	NP_001257450.1:n.4078-4927G>A
NM_001270521.2:c.4078-4927G>A (MED23)	NP_001257450.1:n.4078-4927G>A
NM_001369020.1:c.242C>T (ARG1)	NP_001355949.1:p.Ala81Val
NM_015979.3:c.4096-4927G>A (MED23)	NP_057063.2:n.4096-4927G>A
NM_015979.4:c.4096-4927G>A (MED23)	NP_057063.2:n.4096-4927G>A
NR_160934.1:n.226C>T (ARG1)
ENST00000275196.5:n.226C>T (ARG1)
ENST00000354577.8:c.4096-4927G>A (MED23)	ENSP00000346588.4:n.4096-4927G>A
ENST00000356962.2:c.266C>T (ARG1)	ENSP00000349446.2:p.Ala89Val
ENST00000368087.7:c.242C>T (ARG1)	ENSP00000357066.3:p.Ala81Val
ENST00000469293.1:n.258C>T (ARG1)
ENST00000484820.1:n.214C>T (ARG1)
ENST00000498260.1:n.283C>T (ARG1)
ENST00000640973.1:c.242C>T (ARG1)	ENSP00000492623.1:p.Ala81Val
ENST00000672052.1:n.489C>T (ARG1)
ENST00000672233.1:c.188C>T (ARG1)	ENSP00000499826.1:p.Ala63Val
ENST00000673234.1:c.*129C>T (ARG1)	ENSP00000499885.1:n.*129C>T
ENST00000673427.1:c.242C>T (ARG1)	ENSP00000500160.1:p.Ala81Val
XM_011535801.1:c.242C>T (ARG1)	XP_011534103.1:p.Ala81Val
XM_011535801.2:c.242C>T (ARG1)	XP_011534103.1:p.Ala81Val