Canonical Allele Identifier: CA452146742

Gene: ARG1

Linked Data

• gnomAD v4: 6-131573324-T-C
• MyVariant Identifiers: chr6:g.131894464T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573324T>C , CM000668.2:g.131573324T>C	GRCh38
NC_000006.11:g.131894464T>C , CM000668.1:g.131894464T>C	GRCh37
NC_000006.10:g.131936157T>C	NCBI36
NG_007086.2:g.5100T>C
NG_031860.1:g.59900A>G
NG_031860.2:g.59900A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.42T>C MANE Select	ENSP00000357066.3:p.Pro14=
ENST00000640973.1:c.42T>C	ENSP00000492623.1:p.Pro14=
ENST00000672052.1:n.305-3339T>C
ENST00000672233.1:c.77-5787T>C	ENSP00000499826.1:n.77-5787T>C
ENST00000673234.1:c.77-3339T>C	ENSP00000499885.1:n.77-3339T>C
ENST00000673427.1:c.42T>C	ENSP00000500160.1:p.Pro14=
ENST00000275196.5:n.99T>C
ENST00000356962.2:c.42T>C	ENSP00000349446.2:p.Pro14=
ENST00000368087.7:c.42T>C	ENSP00000357066.3:p.Pro14=
ENST00000469293.1:n.131T>C
ENST00000498260.1:n.83T>C
NM_000045.3:c.42T>C	NP_000036.2:p.Pro14=
NM_001244438.1:c.42T>C	NP_001231367.1:p.Pro14=
XM_011535801.1:c.42T>C	XP_011534103.1:p.Pro14=
XM_011535801.2:c.42T>C	XP_011534103.1:p.Pro14=
NM_000045.4:c.42T>C MANE Select	NP_000036.2:p.Pro14=
NM_001244438.2:c.42T>C	NP_001231367.1:p.Pro14=
NM_001369020.1:c.42T>C	NP_001355949.1:p.Pro14=
NR_160934.1:n.99T>C