Canonical Allele Identifier: CA415759049

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985916C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050536C>A , CM000663.2:g.1050536C>A	GRCh38
NC_000001.10:g.985916C>A , CM000663.1:g.985916C>A	GRCh37
NC_000001.9:g.975779C>A	NCBI36
NG_016346.1:g.35414C>A , LRG_198:g.35414C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.5086C>A MANE Select	ENSP00000368678.2:p.Arg1696=
ENST00000651234.1:c.4771C>A	ENSP00000499046.1:p.Arg1591=
ENST00000652369.1:c.4771C>A	ENSP00000498543.1:p.Arg1591=
ENST00000379370.6:c.5086C>A	ENSP00000368678.2:p.Arg1696=
ENST00000620552.4:c.4672C>A	ENSP00000484607.1:p.Arg1558=
NM_001305275.1:c.5086C>A	NP_001292204.1:p.Arg1696=
NM_198576.3:c.5086C>A	NP_940978.2:p.Arg1696=
XM_005244749.2:c.5086C>A	XP_005244806.1:p.Arg1696=
XM_006710635.2:c.5086C>A	XP_006710698.1:p.Arg1696=
XM_011541429.1:c.5086C>A	XP_011539731.1:p.Arg1696=
XM_011541430.1:c.4213C>A	XP_011539732.1:p.Arg1405=
XM_011541431.1:c.3352C>A	XP_011539733.1:p.Arg1118=
XR_946650.1:n.5153C>A
NM_001364727.1:c.4771C>A	NP_001351656.1:p.Arg1591=
XM_005244749.3:c.5086C>A	XP_005244806.1:p.Arg1696=
XM_011541429.2:c.5086C>A	XP_011539731.1:p.Arg1696=
XR_946650.2:n.5157C>A
NM_001305275.2:c.5086C>A	NP_001292204.1:p.Arg1696=
NM_198576.4:c.5086C>A MANE Select	NP_940978.2:p.Arg1696=
NM_001364727.2:c.4771C>A	NP_001351656.1:p.Arg1591=