Canonical Allele Identifier: CA2578740848

Gene: ARG1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573247G>T , CM000668.2:g.131573247G>T	GRCh38
NC_000006.11:g.131894387G>T , CM000668.1:g.131894387G>T	GRCh37
NC_000006.10:g.131936080G>T	NCBI36
NG_007086.2:g.5023G>T
NG_031860.1:g.59977C>A
NG_031860.2:g.59977C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368087.8:c.-36G>T MANE Select	ENSP00000357066.3:n.-36G>T
ENST00000672052.1:n.305-3416G>T
ENST00000672233.1:c.77-5864G>T	ENSP00000499826.1:n.77-5864G>T
ENST00000673234.1:c.77-3416G>T	ENSP00000499885.1:n.77-3416G>T
ENST00000673427.1:c.-36G>T	ENSP00000500160.1:n.-36G>T
ENST00000275196.5:n.22G>T
ENST00000356962.2:c.-36G>T	ENSP00000349446.2:n.-36G>T
ENST00000368087.7:c.-36G>T	ENSP00000357066.3:n.-36G>T
ENST00000469293.1:n.54G>T
ENST00000498260.1:n.6G>T
NM_000045.3:c.-36G>T	NP_000036.2:n.-36G>T
NM_001244438.1:c.-36G>T	NP_001231367.1:n.-36G>T
XM_011535801.1:c.-36G>T	XP_011534103.1:n.-36G>T
XM_011535801.2:c.-36G>T	XP_011534103.1:n.-36G>T
NM_000045.4:c.-36G>T MANE Select	NP_000036.2:n.-36G>T
NM_001244438.2:c.-36G>T	NP_001231367.1:n.-36G>T
NM_001369020.1:c.-36G>T	NP_001355949.1:n.-36G>T
NR_160934.1:n.22G>T