Canonical Allele Identifier: CA1664135527

Gene: ARG1 MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131581417T= , CM000668.2:g.131581417T=	GRCh38
NC_000006.11:g.131902557T= , CM000668.1:g.131902557T=	GRCh37
NC_000006.10:g.131944250T=	NCBI36
NG_007086.2:g.13193T=
NG_031860.1:g.51807A=
NG_031860.2:g.51807A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.465+39T= (ARG1) MANE Select	ENSP00000357066.3:n.465+39T=
ENST00000640973.1:c.465+39T= (ARG1)	ENSP00000492623.1:n.465+39T=
ENST00000672233.1:c.411+39T= (ARG1)	ENSP00000499826.1:n.411+39T=
ENST00000673234.1:c.*352+39T= (ARG1)	ENSP00000499885.1:n.*352+39T=
ENST00000673427.1:c.306-1643T= (ARG1)	ENSP00000500160.1:n.306-1643T=
ENST00000275196.5:n.449+39T= (ARG1)
ENST00000354577.8:c.4095+6292A= (MED23)	ENSP00000346588.4:n.4095+6292A=
ENST00000356962.2:c.489+39T= (ARG1)	ENSP00000349446.2:n.489+39T=
ENST00000368087.7:c.465+39T= (ARG1)	ENSP00000357066.3:n.465+39T=
NM_000045.3:c.465+39T= (ARG1)	NP_000036.2:n.465+39T=
NM_001244438.1:c.489+39T= (ARG1)	NP_001231367.1:n.489+39T=
NM_001270521.1:c.4077+6292A= (MED23)	NP_001257450.1:n.4077+6292A=
NM_015979.3:c.4095+6292A= (MED23)	NP_057063.2:n.4095+6292A=
XM_011535801.1:c.306-1643T= (ARG1)	XP_011534103.1:n.306-1643T=
XM_011535801.2:c.306-1643T= (ARG1)	XP_011534103.1:n.306-1643T=
NM_000045.4:c.465+39T= (ARG1) MANE Select	NP_000036.2:n.465+39T=
NM_001244438.2:c.489+39T= (ARG1)	NP_001231367.1:n.489+39T=
NM_001270521.2:c.4077+6292A= (MED23)	NP_001257450.1:n.4077+6292A=
NM_001369020.1:c.306-1643T= (ARG1)	NP_001355949.1:n.306-1643T=
NM_015979.4:c.4095+6292A= (MED23)	NP_057063.2:n.4095+6292A=
NR_160934.1:n.449+39T= (ARG1)