Canonical Allele Identifier: CA365653587

Gene: ARG1 MED23

Linked Data

• gnomAD v4: 6-131583793-C-T
• MyVariant Identifiers: chr6:g.131904933C>T (hg19) ; chr6:g.131583793C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131583793C>T , CM000668.2:g.131583793C>T	GRCh38
NC_000006.11:g.131904933C>T , CM000668.1:g.131904933C>T	GRCh37
NC_000006.10:g.131946626C>T	NCBI36
NG_007086.2:g.15569C>T
NG_031860.1:g.49431G>A
NG_031860.2:g.49431G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.854C>T (ARG1) MANE Select	ENSP00000357066.3:p.Thr285Ile
ENST00000640973.1:c.605-9C>T (ARG1)	ENSP00000492623.1:n.605-9C>T
ENST00000672233.1:c.800C>T (ARG1)	ENSP00000499826.1:p.Thr267Ile
ENST00000673234.1:c.*741C>T (ARG1)	ENSP00000499885.1:n.*741C>T
ENST00000673427.1:c.599C>T (ARG1)	ENSP00000500160.1:p.Thr200Ile
ENST00000354577.8:c.4095+3916G>A (MED23)	ENSP00000346588.4:n.4095+3916G>A
ENST00000356962.2:c.878C>T (ARG1)	ENSP00000349446.2:p.Thr293Ile
ENST00000368087.7:c.854C>T (ARG1)	ENSP00000357066.3:p.Thr285Ile
NM_000045.3:c.854C>T (ARG1)	NP_000036.2:p.Thr285Ile
NM_001244438.1:c.878C>T (ARG1)	NP_001231367.1:p.Thr293Ile
NM_001270521.1:c.4077+3916G>A (MED23)	NP_001257450.1:n.4077+3916G>A
NM_015979.3:c.4095+3916G>A (MED23)	NP_057063.2:n.4095+3916G>A
XM_011535801.1:c.599C>T (ARG1)	XP_011534103.1:p.Thr200Ile
XM_011535801.2:c.599C>T (ARG1)	XP_011534103.1:p.Thr200Ile
NM_000045.4:c.854C>T (ARG1) MANE Select	NP_000036.2:p.Thr285Ile
NM_001244438.2:c.878C>T (ARG1)	NP_001231367.1:p.Thr293Ile
NM_001270521.2:c.4077+3916G>A (MED23)	NP_001257450.1:n.4077+3916G>A
NM_001369020.1:c.599C>T (ARG1)	NP_001355949.1:p.Thr200Ile
NM_015979.4:c.4095+3916G>A (MED23)	NP_057063.2:n.4095+3916G>A
NR_160934.1:n.838C>T (ARG1)