Canonical Allele Identifier: CA2642492092

Gene: AGRN

Linked Data

• gnomAD v4: 1-1050082-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050082A>C , CM000663.2:g.1050082A>C	GRCh38
NC_000001.10:g.985462A>C , CM000663.1:g.985462A>C	GRCh37
NC_000001.9:g.975325A>C	NCBI36
NG_016346.1:g.34960A>C , LRG_198:g.34960A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4879+45A>C MANE Select	ENSP00000368678.2:n.4879+45A>C
ENST00000651234.1:c.4564+45A>C	ENSP00000499046.1:n.4564+45A>C
ENST00000652369.1:c.4564+45A>C	ENSP00000498543.1:n.4564+45A>C
ENST00000379370.6:c.4879+45A>C	ENSP00000368678.2:n.4879+45A>C
ENST00000620552.4:c.4465+45A>C	ENSP00000484607.1:n.4465+45A>C
NM_001305275.1:c.4879+45A>C	NP_001292204.1:n.4879+45A>C
NM_198576.3:c.4879+45A>C	NP_940978.2:n.4879+45A>C
XM_005244749.2:c.4879+45A>C	XP_005244806.1:n.4879+45A>C
XM_006710635.2:c.4879+45A>C	XP_006710698.1:n.4879+45A>C
XM_011541429.1:c.4879+45A>C	XP_011539731.1:n.4879+45A>C
XM_011541430.1:c.4006+45A>C	XP_011539732.1:n.4006+45A>C
XM_011541431.1:c.3145+45A>C	XP_011539733.1:n.3145+45A>C
XR_946650.1:n.4946+45A>C
NM_001364727.1:c.4564+45A>C	NP_001351656.1:n.4564+45A>C
XM_005244749.3:c.4879+45A>C	XP_005244806.1:n.4879+45A>C
XM_011541429.2:c.4879+45A>C	XP_011539731.1:n.4879+45A>C
XR_946650.2:n.4950+45A>C
NM_001305275.2:c.4879+45A>C	NP_001292204.1:n.4879+45A>C
NM_198576.4:c.4879+45A>C MANE Select	NP_940978.2:n.4879+45A>C
NM_001364727.2:c.4564+45A>C	NP_001351656.1:n.4564+45A>C