Canonical Allele Identifier: CA415758272

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983402T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048022T>A , CM000663.2:g.1048022T>A	GRCh38
NC_000001.10:g.983402T>A , CM000663.1:g.983402T>A	GRCh37
NC_000001.9:g.973265T>A	NCBI36
NG_016346.1:g.32900T>A , LRG_198:g.32900T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3762T>A MANE Select	ENSP00000368678.2:p.Pro1254=
ENST00000651234.1:c.3447T>A	ENSP00000499046.1:p.Pro1149=
ENST00000652369.1:c.3447T>A	ENSP00000498543.1:p.Pro1149=
ENST00000379370.6:c.3762T>A	ENSP00000368678.2:p.Pro1254=
ENST00000620552.4:c.3348T>A	ENSP00000484607.1:p.Pro1116=
NM_001305275.1:c.3762T>A	NP_001292204.1:p.Pro1254=
NM_198576.3:c.3762T>A	NP_940978.2:p.Pro1254=
XM_005244749.2:c.3762T>A	XP_005244806.1:p.Pro1254=
XM_006710635.2:c.3762T>A	XP_006710698.1:p.Pro1254=
XM_011541429.1:c.3762T>A	XP_011539731.1:p.Pro1254=
XM_011541430.1:c.2889T>A	XP_011539732.1:p.Pro963=
XM_011541431.1:c.2028T>A	XP_011539733.1:p.Pro676=
XR_946650.1:n.3829T>A
NM_001364727.1:c.3447T>A	NP_001351656.1:p.Pro1149=
XM_005244749.3:c.3762T>A	XP_005244806.1:p.Pro1254=
XM_011541429.2:c.3762T>A	XP_011539731.1:p.Pro1254=
XR_946650.2:n.3833T>A
NM_001305275.2:c.3762T>A	NP_001292204.1:p.Pro1254=
NM_198576.4:c.3762T>A MANE Select	NP_940978.2:p.Pro1254=
NM_001364727.2:c.3447T>A	NP_001351656.1:p.Pro1149=