Canonical Allele Identifier: CA1664137584

Gene: ARG1 MED23

Linked Data

• dbSNP Id: rs1774050386

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131583567_131583568insACCAAG , CM000668.2:g.131583567_131583568insACCAAG	GRCh38
NC_000006.11:g.131904707_131904708insACCAAG , CM000668.1:g.131904707_131904708insACCAAG	GRCh37
NC_000006.10:g.131946400_131946401insACCAAG	NCBI36
NG_007086.2:g.15343_15344insACCAAG
NG_031860.1:g.49656_49657insCTTGGT
NG_031860.2:g.49656_49657insCTTGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.802+76_802+77insACCAAG (ARG1) MANE Select	ENSP00000357066.3:n.802+76_802+77insACCAAG
ENST00000640973.1:c.605-235_605-234insACCAAG (ARG1)	ENSP00000492623.1:n.605-235_605-234insACCAAG
ENST00000672233.1:c.748+76_748+77insACCAAG (ARG1)	ENSP00000499826.1:n.748+76_748+77insACCAAG
ENST00000673234.1:c.*689+76_*689+77insACCAAG (ARG1)	ENSP00000499885.1:n.*689+76_*689+77insACCAAG
ENST00000673427.1:c.547+76_547+77insACCAAG (ARG1)	ENSP00000500160.1:n.547+76_547+77insACCAAG
ENST00000354577.8:c.4095+4141_4095+4142insCTTGGT (MED23)	ENSP00000346588.4:n.4095+4141_4095+4142insCTTGGT
ENST00000356962.2:c.826+76_826+77insACCAAG (ARG1)	ENSP00000349446.2:n.826+76_826+77insACCAAG
ENST00000368087.7:c.802+76_802+77insACCAAG (ARG1)	ENSP00000357066.3:n.802+76_802+77insACCAAG
NM_000045.3:c.802+76_802+77insACCAAG (ARG1)	NP_000036.2:n.802+76_802+77insACCAAG
NM_001244438.1:c.826+76_826+77insACCAAG (ARG1)	NP_001231367.1:n.826+76_826+77insACCAAG
NM_001270521.1:c.4077+4141_4077+4142insCTTGGT (MED23)	NP_001257450.1:n.4077+4141_4077+4142insCTTGGT
NM_015979.3:c.4095+4141_4095+4142insCTTGGT (MED23)	NP_057063.2:n.4095+4141_4095+4142insCTTGGT
XM_011535801.1:c.547+76_547+77insACCAAG (ARG1)	XP_011534103.1:n.547+76_547+77insACCAAG
XM_011535801.2:c.547+76_547+77insACCAAG (ARG1)	XP_011534103.1:n.547+76_547+77insACCAAG
NM_000045.4:c.802+76_802+77insACCAAG (ARG1) MANE Select	NP_000036.2:n.802+76_802+77insACCAAG
NM_001244438.2:c.826+76_826+77insACCAAG (ARG1)	NP_001231367.1:n.826+76_826+77insACCAAG
NM_001270521.2:c.4077+4141_4077+4142insCTTGGT (MED23)	NP_001257450.1:n.4077+4141_4077+4142insCTTGGT
NM_001369020.1:c.547+76_547+77insACCAAG (ARG1)	NP_001355949.1:n.547+76_547+77insACCAAG
NM_015979.4:c.4095+4141_4095+4142insCTTGGT (MED23)	NP_057063.2:n.4095+4141_4095+4142insCTTGGT
NR_160934.1:n.786+76_786+77insACCAAG (ARG1)