Canonical Allele Identifier: CA127981

Gene: AGRN

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050575G>C , CM000663.2:g.1050575G>C	GRCh38
NC_000001.10:g.985955G>C , CM000663.1:g.985955G>C	GRCh37
NC_000001.9:g.975818G>C	NCBI36
NG_016346.1:g.35453G>C , LRG_198:g.35453G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.5125G>C MANE Select	ENSP00000368678.2:p.Gly1709Arg
ENST00000651234.1:c.4810G>C	ENSP00000499046.1:p.Gly1604Arg
ENST00000652369.1:c.4810G>C	ENSP00000498543.1:p.Gly1604Arg
ENST00000379370.6:c.5125G>C	ENSP00000368678.2:p.Gly1709Arg
ENST00000419249.1:c.20G>C
ENST00000620552.4:c.4711G>C	ENSP00000484607.1:p.Gly1571Arg
NM_001305275.1:c.5125G>C	NP_001292204.1:p.Gly1709Arg
NM_198576.3:c.5125G>C	NP_940978.2:p.Gly1709Arg
XM_005244749.2:c.5125G>C	XP_005244806.1:p.Gly1709Arg
XM_006710635.2:c.5125G>C	XP_006710698.1:p.Gly1709Arg
XM_011541429.1:c.5125G>C	XP_011539731.1:p.Gly1709Arg
XM_011541430.1:c.4252G>C	XP_011539732.1:p.Gly1418Arg
XM_011541431.1:c.3391G>C	XP_011539733.1:p.Gly1131Arg
XR_946650.1:n.5192G>C
NM_001364727.1:c.4810G>C	NP_001351656.1:p.Gly1604Arg
XM_005244749.3:c.5125G>C	XP_005244806.1:p.Gly1709Arg
XM_011541429.2:c.5125G>C	XP_011539731.1:p.Gly1709Arg
XR_946650.2:n.5196G>C
NM_001305275.2:c.5125G>C	NP_001292204.1:p.Gly1709Arg
NM_198576.4:c.5125G>C MANE Select	NP_940978.2:p.Gly1709Arg
NM_001364727.2:c.4810G>C	NP_001351656.1:p.Gly1604Arg