Canonical Allele Identifier: CA337851590

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983236A>T (hg19) ; chr1:g.1047856A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047856A>T , CM000663.2:g.1047856A>T	GRCh38
NC_000001.10:g.983236A>T , CM000663.1:g.983236A>T	GRCh37
NC_000001.9:g.973099A>T	NCBI36
NG_016346.1:g.32734A>T , LRG_198:g.32734A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3712A>T MANE Select	ENSP00000368678.2:p.Arg1238Trp
ENST00000651234.1:c.3397A>T	ENSP00000499046.1:p.Arg1133Trp
ENST00000652369.1:c.3397A>T	ENSP00000498543.1:p.Arg1133Trp
ENST00000379370.6:c.3712A>T	ENSP00000368678.2:p.Arg1238Trp
ENST00000466223.1:n.450A>T
ENST00000620552.4:c.3298A>T	ENSP00000484607.1:p.Arg1100Trp
NM_001305275.1:c.3712A>T	NP_001292204.1:p.Arg1238Trp
NM_198576.3:c.3712A>T	NP_940978.2:p.Arg1238Trp
XM_005244749.2:c.3712A>T	XP_005244806.1:p.Arg1238Trp
XM_006710635.2:c.3712A>T	XP_006710698.1:p.Arg1238Trp
XM_011541429.1:c.3712A>T	XP_011539731.1:p.Arg1238Trp
XM_011541430.1:c.2839A>T	XP_011539732.1:p.Arg947Trp
XM_011541431.1:c.1978A>T	XP_011539733.1:p.Arg660Trp
XR_946650.1:n.3779A>T
NM_001364727.1:c.3397A>T	NP_001351656.1:p.Arg1133Trp
XM_005244749.3:c.3712A>T	XP_005244806.1:p.Arg1238Trp
XM_011541429.2:c.3712A>T	XP_011539731.1:p.Arg1238Trp
XR_946650.2:n.3783A>T
NM_001305275.2:c.3712A>T	NP_001292204.1:p.Arg1238Trp
NM_198576.4:c.3712A>T MANE Select	NP_940978.2:p.Arg1238Trp
NM_001364727.2:c.3397A>T	NP_001351656.1:p.Arg1133Trp