Canonical Allele Identifier: CA2642492142

Gene: AGRN

Linked Data

• gnomAD v4: 1-1050122-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050122A>T , CM000663.2:g.1050122A>T	GRCh38
NC_000001.10:g.985502A>T , CM000663.1:g.985502A>T	GRCh37
NC_000001.9:g.975365A>T	NCBI36
NG_016346.1:g.35000A>T , LRG_198:g.35000A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4879+85A>T MANE Select	ENSP00000368678.2:n.4879+85A>T
ENST00000651234.1:c.4564+85A>T	ENSP00000499046.1:n.4564+85A>T
ENST00000652369.1:c.4564+85A>T	ENSP00000498543.1:n.4564+85A>T
ENST00000379370.6:c.4879+85A>T	ENSP00000368678.2:n.4879+85A>T
ENST00000620552.4:c.4465+85A>T	ENSP00000484607.1:n.4465+85A>T
NM_001305275.1:c.4879+85A>T	NP_001292204.1:n.4879+85A>T
NM_198576.3:c.4879+85A>T	NP_940978.2:n.4879+85A>T
XM_005244749.2:c.4879+85A>T	XP_005244806.1:n.4879+85A>T
XM_006710635.2:c.4879+85A>T	XP_006710698.1:n.4879+85A>T
XM_011541429.1:c.4879+85A>T	XP_011539731.1:n.4879+85A>T
XM_011541430.1:c.4006+85A>T	XP_011539732.1:n.4006+85A>T
XM_011541431.1:c.3145+85A>T	XP_011539733.1:n.3145+85A>T
XR_946650.1:n.4946+85A>T
NM_001364727.1:c.4564+85A>T	NP_001351656.1:n.4564+85A>T
XM_005244749.3:c.4879+85A>T	XP_005244806.1:n.4879+85A>T
XM_011541429.2:c.4879+85A>T	XP_011539731.1:n.4879+85A>T
XR_946650.2:n.4950+85A>T
NM_001305275.2:c.4879+85A>T	NP_001292204.1:n.4879+85A>T
NM_198576.4:c.4879+85A>T MANE Select	NP_940978.2:n.4879+85A>T
NM_001364727.2:c.4564+85A>T	NP_001351656.1:n.4564+85A>T