Canonical Allele Identifier: CA337851669

Gene: AGRN

Linked Data

• ClinVar Variation Id: 1409137
• ClinVar RCV Id: RCV001909685
• dbSNP Id: rs142620337
• gnomAD v2: 1-983243-C-A
• gnomAD v3: 1-1047863-C-A
• gnomAD v4: 1-1047863-C-A
• MyVariant Identifiers: chr1:g.983243C>A (hg19) ; chr1:g.1047863C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047863C>A , CM000663.2:g.1047863C>A	GRCh38
NC_000001.10:g.983243C>A , CM000663.1:g.983243C>A	GRCh37
NC_000001.9:g.973106C>A	NCBI36
NG_016346.1:g.32741C>A , LRG_198:g.32741C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3719C>A MANE Select	ENSP00000368678.2:p.Pro1240Gln
ENST00000651234.1:c.3404C>A	ENSP00000499046.1:p.Pro1135Gln
ENST00000652369.1:c.3404C>A	ENSP00000498543.1:p.Pro1135Gln
ENST00000379370.6:c.3719C>A	ENSP00000368678.2:p.Pro1240Gln
ENST00000466223.1:n.457C>A
ENST00000620552.4:c.3305C>A	ENSP00000484607.1:p.Pro1102Gln
NM_001305275.1:c.3719C>A	NP_001292204.1:p.Pro1240Gln
NM_198576.3:c.3719C>A	NP_940978.2:p.Pro1240Gln
XM_005244749.2:c.3719C>A	XP_005244806.1:p.Pro1240Gln
XM_006710635.2:c.3719C>A	XP_006710698.1:p.Pro1240Gln
XM_011541429.1:c.3719C>A	XP_011539731.1:p.Pro1240Gln
XM_011541430.1:c.2846C>A	XP_011539732.1:p.Pro949Gln
XM_011541431.1:c.1985C>A	XP_011539733.1:p.Pro662Gln
XR_946650.1:n.3786C>A
NM_001364727.1:c.3404C>A	NP_001351656.1:p.Pro1135Gln
XM_005244749.3:c.3719C>A	XP_005244806.1:p.Pro1240Gln
XM_011541429.2:c.3719C>A	XP_011539731.1:p.Pro1240Gln
XR_946650.2:n.3790C>A
NM_001305275.2:c.3719C>A	NP_001292204.1:p.Pro1240Gln
NM_198576.4:c.3719C>A MANE Select	NP_940978.2:p.Pro1240Gln
NM_001364727.2:c.3404C>A	NP_001351656.1:p.Pro1135Gln