Canonical Allele Identifier: CA3999245

Gene: ARG1 MED23

Linked Data

• dbSNP Id: rs747268449
• ExAC: 6:131902429 C / T
• gnomAD v2: 6-131902429-C-T
• gnomAD v4: 6-131581289-C-T
• MyVariant Identifiers: chr6:g.131902429C>T (hg19) ; chr6:g.131581289C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131581289C>T , CM000668.2:g.131581289C>T	GRCh38
NC_000006.11:g.131902429C>T , CM000668.1:g.131902429C>T	GRCh37
NC_000006.10:g.131944122C>T	NCBI36
NG_007086.2:g.13065C>T
NG_031860.1:g.51935G>A
NG_031860.2:g.51935G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368087.8:c.376C>T (ARG1) MANE Select	ENSP00000357066.3:p.His126Tyr
ENST00000640973.1:c.376C>T (ARG1)	ENSP00000492623.1:p.His126Tyr
ENST00000672233.1:c.322C>T (ARG1)	ENSP00000499826.1:p.His108Tyr
ENST00000673234.1:c.*263C>T (ARG1)	ENSP00000499885.1:n.*263C>T
ENST00000673427.1:c.306-1771C>T (ARG1)	ENSP00000500160.1:n.306-1771C>T
ENST00000275196.5:n.360C>T (ARG1)
ENST00000354577.8:c.4095+6420G>A (MED23)	ENSP00000346588.4:n.4095+6420G>A
ENST00000356962.2:c.400C>T (ARG1)	ENSP00000349446.2:p.His134Tyr
ENST00000368087.7:c.376C>T (ARG1)	ENSP00000357066.3:p.His126Tyr
NM_000045.3:c.376C>T (ARG1)	NP_000036.2:p.His126Tyr
NM_001244438.1:c.400C>T (ARG1)	NP_001231367.1:p.His134Tyr
NM_001270521.1:c.4077+6420G>A (MED23)	NP_001257450.1:n.4077+6420G>A
NM_015979.3:c.4095+6420G>A (MED23)	NP_057063.2:n.4095+6420G>A
XM_011535801.1:c.306-1771C>T (ARG1)	XP_011534103.1:n.306-1771C>T
XM_011535801.2:c.306-1771C>T (ARG1)	XP_011534103.1:n.306-1771C>T
NM_000045.4:c.376C>T (ARG1) MANE Select	NP_000036.2:p.His126Tyr
NM_001244438.2:c.400C>T (ARG1)	NP_001231367.1:p.His134Tyr
NM_001270521.2:c.4077+6420G>A (MED23)	NP_001257450.1:n.4077+6420G>A
NM_001369020.1:c.306-1771C>T (ARG1)	NP_001355949.1:n.306-1771C>T
NM_015979.4:c.4095+6420G>A (MED23)	NP_057063.2:n.4095+6420G>A
NR_160934.1:n.360C>T (ARG1)