Canonical Allele Identifier: CA1664137772

Gene: ARG1 MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131583770A= , CM000668.2:g.131583770A=	GRCh38
NC_000006.11:g.131904910A= , CM000668.1:g.131904910A=	GRCh37
NC_000006.10:g.131946603A=	NCBI36
NG_007086.2:g.15546A=
NG_031860.1:g.49454T=
NG_031860.2:g.49454T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.831A= (ARG1) MANE Select	ENSP00000357066.3:p.Glu277=
ENST00000640973.1:c.605-32A= (ARG1)	ENSP00000492623.1:n.605-32A=
ENST00000672233.1:c.777A= (ARG1)	ENSP00000499826.1:p.Glu259=
ENST00000673234.1:c.*718A= (ARG1)	ENSP00000499885.1:n.*718A=
ENST00000673427.1:c.576A= (ARG1)	ENSP00000500160.1:p.Glu192=
ENST00000354577.8:c.4095+3939T= (MED23)	ENSP00000346588.4:n.4095+3939T=
ENST00000356962.2:c.855A= (ARG1)	ENSP00000349446.2:p.Glu285=
ENST00000368087.7:c.831A= (ARG1)	ENSP00000357066.3:p.Glu277=
NM_000045.3:c.831A= (ARG1)	NP_000036.2:p.Glu277=
NM_001244438.1:c.855A= (ARG1)	NP_001231367.1:p.Glu285=
NM_001270521.1:c.4077+3939T= (MED23)	NP_001257450.1:n.4077+3939T=
NM_015979.3:c.4095+3939T= (MED23)	NP_057063.2:n.4095+3939T=
XM_011535801.1:c.576A= (ARG1)	XP_011534103.1:p.Glu192=
XM_011535801.2:c.576A= (ARG1)	XP_011534103.1:p.Glu192=
NM_000045.4:c.831A= (ARG1) MANE Select	NP_000036.2:p.Glu277=
NM_001244438.2:c.855A= (ARG1)	NP_001231367.1:p.Glu285=
NM_001270521.2:c.4077+3939T= (MED23)	NP_001257450.1:n.4077+3939T=
NM_001369020.1:c.576A= (ARG1)	NP_001355949.1:p.Glu192=
NM_015979.4:c.4095+3939T= (MED23)	NP_057063.2:n.4095+3939T=
NR_160934.1:n.815A= (ARG1)