Canonical Allele Identifier: CA365649212

Gene: ARG1

Linked Data

• MyVariant Identifiers: chr6:g.131894463C>T (hg19) ; chr6:g.131573323C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573323C>T , CM000668.2:g.131573323C>T	GRCh38
NC_000006.11:g.131894463C>T , CM000668.1:g.131894463C>T	GRCh37
NC_000006.10:g.131936156C>T	NCBI36
NG_007086.2:g.5099C>T
NG_031860.1:g.59901G>A
NG_031860.2:g.59901G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.41C>T MANE Select	ENSP00000357066.3:p.Pro14Leu
ENST00000640973.1:c.41C>T	ENSP00000492623.1:p.Pro14Leu
ENST00000672052.1:n.305-3340C>T
ENST00000672233.1:c.77-5788C>T	ENSP00000499826.1:n.77-5788C>T
ENST00000673234.1:c.77-3340C>T	ENSP00000499885.1:n.77-3340C>T
ENST00000673427.1:c.41C>T	ENSP00000500160.1:p.Pro14Leu
ENST00000275196.5:n.98C>T
ENST00000356962.2:c.41C>T	ENSP00000349446.2:p.Pro14Leu
ENST00000368087.7:c.41C>T	ENSP00000357066.3:p.Pro14Leu
ENST00000469293.1:n.130C>T
ENST00000498260.1:n.82C>T
NM_000045.3:c.41C>T	NP_000036.2:p.Pro14Leu
NM_001244438.1:c.41C>T	NP_001231367.1:p.Pro14Leu
XM_011535801.1:c.41C>T	XP_011534103.1:p.Pro14Leu
XM_011535801.2:c.41C>T	XP_011534103.1:p.Pro14Leu
NM_000045.4:c.41C>T MANE Select	NP_000036.2:p.Pro14Leu
NM_001244438.2:c.41C>T	NP_001231367.1:p.Pro14Leu
NM_001369020.1:c.41C>T	NP_001355949.1:p.Pro14Leu
NR_160934.1:n.98C>T