Canonical Allele Identifier: CA1664135561

Gene: ARG1 MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131581470_131581473delinsATTC , CM000668.2:g.131581470_131581473delinsATTC	GRCh38
NC_000006.11:g.131902610_131902613delinsATTC , CM000668.1:g.131902610_131902613delinsATTC	GRCh37
NC_000006.10:g.131944303_131944306delinsATTC	NCBI36
NG_007086.2:g.13246_13249delinsATTC
NG_031860.1:g.51751_51754delinsGAAT
NG_031860.2:g.51751_51754delinsGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.465+92_465+95delinsATTC (ARG1) MANE Select	ENSP00000357066.3:n.465+92_465+95delinsATTC
ENST00000640973.1:c.465+92_465+95delinsATTC (ARG1)	ENSP00000492623.1:n.465+92_465+95delinsATTC
ENST00000672233.1:c.411+92_411+95delinsATTC (ARG1)	ENSP00000499826.1:n.411+92_411+95delinsATTC
ENST00000673234.1:c.*352+92_*352+95delinsATTC (ARG1)	ENSP00000499885.1:n.*352+92_*352+95delinsATTC
ENST00000673427.1:c.306-1590_306-1587delinsATTC (ARG1)	ENSP00000500160.1:n.306-1590_306-1587delinsATTC
ENST00000275196.5:n.449+92_449+95delinsATTC (ARG1)
ENST00000354577.8:c.4095+6236_4095+6239delinsGAAT (MED23)	ENSP00000346588.4:n.4095+6236_4095+6239delinsGAAT
ENST00000356962.2:c.489+92_489+95delinsATTC (ARG1)	ENSP00000349446.2:n.489+92_489+95delinsATTC
ENST00000368087.7:c.465+92_465+95delinsATTC (ARG1)	ENSP00000357066.3:n.465+92_465+95delinsATTC
NM_000045.3:c.465+92_465+95delinsATTC (ARG1)	NP_000036.2:n.465+92_465+95delinsATTC
NM_001244438.1:c.489+92_489+95delinsATTC (ARG1)	NP_001231367.1:n.489+92_489+95delinsATTC
NM_001270521.1:c.4077+6236_4077+6239delinsGAAT (MED23)	NP_001257450.1:n.4077+6236_4077+6239delinsGAAT
NM_015979.3:c.4095+6236_4095+6239delinsGAAT (MED23)	NP_057063.2:n.4095+6236_4095+6239delinsGAAT
XM_011535801.1:c.306-1590_306-1587delinsATTC (ARG1)	XP_011534103.1:n.306-1590_306-1587delinsATTC
XM_011535801.2:c.306-1590_306-1587delinsATTC (ARG1)	XP_011534103.1:n.306-1590_306-1587delinsATTC
NM_000045.4:c.465+92_465+95delinsATTC (ARG1) MANE Select	NP_000036.2:n.465+92_465+95delinsATTC
NM_001244438.2:c.489+92_489+95delinsATTC (ARG1)	NP_001231367.1:n.489+92_489+95delinsATTC
NM_001270521.2:c.4077+6236_4077+6239delinsGAAT (MED23)	NP_001257450.1:n.4077+6236_4077+6239delinsGAAT
NM_001369020.1:c.306-1590_306-1587delinsATTC (ARG1)	NP_001355949.1:n.306-1590_306-1587delinsATTC
NM_015979.4:c.4095+6236_4095+6239delinsGAAT (MED23)	NP_057063.2:n.4095+6236_4095+6239delinsGAAT
NR_160934.1:n.449+92_449+95delinsATTC (ARG1)