Canonical Allele Identifier: CA365653783

Gene: ARG1 MED23

Linked Data

• MyVariant Identifiers: chr6:g.131905035A>C (hg19) ; chr6:g.131583895A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131583895A>C , CM000668.2:g.131583895A>C	GRCh38
NC_000006.11:g.131905035A>C , CM000668.1:g.131905035A>C	GRCh37
NC_000006.10:g.131946728A>C	NCBI36
NG_007086.2:g.15671A>C
NG_031860.1:g.49329T>G
NG_031860.2:g.49329T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.956A>C (ARG1) MANE Select	ENSP00000357066.3:p.Asn319Thr
ENST00000640973.1:c.698A>C (ARG1)	ENSP00000492623.1:p.Asn233Thr
ENST00000672233.1:c.902A>C (ARG1)	ENSP00000499826.1:p.Asn301Thr
ENST00000673234.1:c.*843A>C (ARG1)	ENSP00000499885.1:n.*843A>C
ENST00000673427.1:c.701A>C (ARG1)	ENSP00000500160.1:p.Asn234Thr
ENST00000354577.8:c.4095+3814T>G (MED23)	ENSP00000346588.4:n.4095+3814T>G
ENST00000356962.2:c.980A>C (ARG1)	ENSP00000349446.2:p.Asn327Thr
ENST00000368087.7:c.956A>C (ARG1)	ENSP00000357066.3:p.Asn319Thr
NM_000045.3:c.956A>C (ARG1)	NP_000036.2:p.Asn319Thr
NM_001244438.1:c.980A>C (ARG1)	NP_001231367.1:p.Asn327Thr
NM_001270521.1:c.4077+3814T>G (MED23)	NP_001257450.1:n.4077+3814T>G
NM_015979.3:c.4095+3814T>G (MED23)	NP_057063.2:n.4095+3814T>G
XM_011535801.1:c.701A>C (ARG1)	XP_011534103.1:p.Asn234Thr
XM_011535801.2:c.701A>C (ARG1)	XP_011534103.1:p.Asn234Thr
NM_000045.4:c.956A>C (ARG1) MANE Select	NP_000036.2:p.Asn319Thr
NM_001244438.2:c.980A>C (ARG1)	NP_001231367.1:p.Asn327Thr
NM_001270521.2:c.4077+3814T>G (MED23)	NP_001257450.1:n.4077+3814T>G
NM_001369020.1:c.701A>C (ARG1)	NP_001355949.1:p.Asn234Thr
NM_015979.4:c.4095+3814T>G (MED23)	NP_057063.2:n.4095+3814T>G
NR_160934.1:n.940A>C (ARG1)