Canonical Allele Identifier: CA2578741082

Gene: ARG1 MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131583582A>G , CM000668.2:g.131583582A>G	GRCh38
NC_000006.11:g.131904722A>G , CM000668.1:g.131904722A>G	GRCh37
NC_000006.10:g.131946415A>G	NCBI36
NG_007086.2:g.15358A>G
NG_031860.1:g.49642T>C
NG_031860.2:g.49642T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368087.8:c.802+91A>G (ARG1) MANE Select	ENSP00000357066.3:n.802+91A>G
ENST00000640973.1:c.605-220A>G (ARG1)	ENSP00000492623.1:n.605-220A>G
ENST00000672233.1:c.748+91A>G (ARG1)	ENSP00000499826.1:n.748+91A>G
ENST00000673234.1:c.*689+91A>G (ARG1)	ENSP00000499885.1:n.*689+91A>G
ENST00000673427.1:c.547+91A>G (ARG1)	ENSP00000500160.1:n.547+91A>G
ENST00000354577.8:c.4095+4127T>C (MED23)	ENSP00000346588.4:n.4095+4127T>C
ENST00000356962.2:c.826+91A>G (ARG1)	ENSP00000349446.2:n.826+91A>G
ENST00000368087.7:c.802+91A>G (ARG1)	ENSP00000357066.3:n.802+91A>G
NM_000045.3:c.802+91A>G (ARG1)	NP_000036.2:n.802+91A>G
NM_001244438.1:c.826+91A>G (ARG1)	NP_001231367.1:n.826+91A>G
NM_001270521.1:c.4077+4127T>C (MED23)	NP_001257450.1:n.4077+4127T>C
NM_015979.3:c.4095+4127T>C (MED23)	NP_057063.2:n.4095+4127T>C
XM_011535801.1:c.547+91A>G (ARG1)	XP_011534103.1:n.547+91A>G
XM_011535801.2:c.547+91A>G (ARG1)	XP_011534103.1:n.547+91A>G
NM_000045.4:c.802+91A>G (ARG1) MANE Select	NP_000036.2:n.802+91A>G
NM_001244438.2:c.826+91A>G (ARG1)	NP_001231367.1:n.826+91A>G
NM_001270521.2:c.4077+4127T>C (MED23)	NP_001257450.1:n.4077+4127T>C
NM_001369020.1:c.547+91A>G (ARG1)	NP_001355949.1:n.547+91A>G
NM_015979.4:c.4095+4127T>C (MED23)	NP_057063.2:n.4095+4127T>C
NR_160934.1:n.786+91A>G (ARG1)