Canonical Allele Identifier: CA2680351450

Gene: ARG1

Linked Data

• gnomAD v4: 6-131573228-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573228C>T , CM000668.2:g.131573228C>T	GRCh38
NC_000006.11:g.131894368C>T , CM000668.1:g.131894368C>T	GRCh37
NC_000006.10:g.131936061C>T	NCBI36
NG_007086.2:g.5004C>T
NG_031860.1:g.59996G>A
NG_031860.2:g.59996G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368087.8:c.-55C>T MANE Select	ENSP00000357066.3:n.-55C>T
ENST00000672052.1:n.305-3435C>T
ENST00000672233.1:c.77-5883C>T	ENSP00000499826.1:n.77-5883C>T
ENST00000673234.1:c.77-3435C>T	ENSP00000499885.1:n.77-3435C>T
ENST00000275196.5:n.3C>T
ENST00000356962.2:c.-55C>T	ENSP00000349446.2:n.-55C>T
ENST00000368087.7:c.-55C>T	ENSP00000357066.3:n.-55C>T
ENST00000469293.1:n.35C>T
NM_000045.3:c.-55C>T	NP_000036.2:n.-55C>T
NM_001244438.1:c.-55C>T	NP_001231367.1:n.-55C>T
XM_011535801.1:c.-55C>T	XP_011534103.1:n.-55C>T
XM_011535801.2:c.-55C>T	XP_011534103.1:n.-55C>T
NM_000045.4:c.-55C>T MANE Select	NP_000036.2:n.-55C>T
NM_001244438.2:c.-55C>T	NP_001231367.1:n.-55C>T
NM_001369020.1:c.-55C>T	NP_001355949.1:n.-55C>T
NR_160934.1:n.3C>T