Canonical Allele Identifier: CA365650586

Gene: ARG1 MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131579201G>T , CM000668.2:g.131579201G>T	GRCh38
NC_000006.11:g.131900341G>T , CM000668.1:g.131900341G>T	GRCh37
NC_000006.10:g.131942034G>T	NCBI36
NG_007086.2:g.10977G>T
NG_031860.1:g.54023C>A
NG_031860.2:g.54023C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000045.4:c.221G>T (ARG1) MANE Select	NP_000036.2:p.Gly74Val
ENST00000368087.8:c.221G>T (ARG1) MANE Select	ENSP00000357066.3:p.Gly74Val
NM_000045.3:c.221G>T (ARG1)	NP_000036.2:p.Gly74Val
NM_001244438.1:c.245G>T (ARG1)	NP_001231367.1:p.Gly82Val
NM_001244438.2:c.245G>T (ARG1)	NP_001231367.1:p.Gly82Val
NM_001270521.1:c.4078-4906C>A (MED23)	NP_001257450.1:n.4078-4906C>A
NM_001270521.2:c.4078-4906C>A (MED23)	NP_001257450.1:n.4078-4906C>A
NM_001369020.1:c.221G>T (ARG1)	NP_001355949.1:p.Gly74Val
NM_015979.3:c.4096-4906C>A (MED23)	NP_057063.2:n.4096-4906C>A
NM_015979.4:c.4096-4906C>A (MED23)	NP_057063.2:n.4096-4906C>A
NR_160934.1:n.205G>T (ARG1)
ENST00000275196.5:n.205G>T (ARG1)
ENST00000354577.8:c.4096-4906C>A (MED23)	ENSP00000346588.4:n.4096-4906C>A
ENST00000356962.2:c.245G>T (ARG1)	ENSP00000349446.2:p.Gly82Val
ENST00000368087.7:c.221G>T (ARG1)	ENSP00000357066.3:p.Gly74Val
ENST00000469293.1:n.237G>T (ARG1)
ENST00000484820.1:n.193G>T (ARG1)
ENST00000498260.1:n.262G>T (ARG1)
ENST00000640973.1:c.221G>T (ARG1)	ENSP00000492623.1:p.Gly74Val
ENST00000672052.1:n.468G>T (ARG1)
ENST00000672233.1:c.167G>T (ARG1)	ENSP00000499826.1:p.Gly56Val
ENST00000673234.1:c.*108G>T (ARG1)	ENSP00000499885.1:n.*108G>T
ENST00000673427.1:c.221G>T (ARG1)	ENSP00000500160.1:p.Gly74Val
XM_011535801.1:c.221G>T (ARG1)	XP_011534103.1:p.Gly74Val
XM_011535801.2:c.221G>T (ARG1)	XP_011534103.1:p.Gly74Val