Canonical Allele Identifier: CA415756079

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.957583T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022203T>A , CM000663.2:g.1022203T>A	GRCh38
NC_000001.10:g.957583T>A , CM000663.1:g.957583T>A	GRCh37
NC_000001.9:g.947446T>A	NCBI36
NG_016346.1:g.7081T>A , LRG_198:g.7081T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.204T>A MANE Select	ENSP00000368678.2:p.Val68=
ENST00000379370.6:c.204T>A	ENSP00000368678.2:p.Val68=
ENST00000620552.4:c.-211T>A	ENSP00000484607.1:n.-211T>A
NM_001305275.1:c.204T>A	NP_001292204.1:p.Val68=
NM_198576.3:c.204T>A	NP_940978.2:p.Val68=
XM_005244749.2:c.204T>A	XP_005244806.1:p.Val68=
XM_006710635.2:c.204T>A	XP_006710698.1:p.Val68=
XM_011541429.1:c.204T>A	XP_011539731.1:p.Val68=
XM_011541430.1:c.204T>A	XP_011539732.1:p.Val68=
XR_946650.1:n.271T>A
XM_005244749.3:c.204T>A	XP_005244806.1:p.Val68=
XM_011541429.2:c.204T>A	XP_011539731.1:p.Val68=
XR_946650.2:n.275T>A
NM_001305275.2:c.204T>A	NP_001292204.1:p.Val68=
NM_198576.4:c.204T>A MANE Select	NP_940978.2:p.Val68=