Canonical Allele Identifier: CA16759799

Gene: AGRN

Linked Data

• dbSNP Id: rs753787358
• gnomAD v3: 1-1047765-C-T
• gnomAD v4: 1-1047765-C-T
• MyVariant Identifiers: chr1:g.983145C>T (hg19) ; chr1:g.1047765C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047765C>T , CM000663.2:g.1047765C>T	GRCh38
NC_000001.10:g.983145C>T , CM000663.1:g.983145C>T	GRCh37
NC_000001.9:g.973008C>T	NCBI36
NG_016346.1:g.32643C>T , LRG_198:g.32643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3632-11C>T MANE Select	ENSP00000368678.2:n.3632-11C>T
ENST00000651234.1:c.3317-11C>T	ENSP00000499046.1:n.3317-11C>T
ENST00000652369.1:c.3317-11C>T	ENSP00000498543.1:n.3317-11C>T
ENST00000379370.6:c.3632-11C>T	ENSP00000368678.2:n.3632-11C>T
ENST00000466223.1:n.370-11C>T
ENST00000478677.1:n.214-11C>T
ENST00000620552.4:c.3218-11C>T	ENSP00000484607.1:n.3218-11C>T
NM_001305275.1:c.3632-11C>T	NP_001292204.1:n.3632-11C>T
NM_198576.3:c.3632-11C>T	NP_940978.2:n.3632-11C>T
XM_005244749.2:c.3632-11C>T	XP_005244806.1:n.3632-11C>T
XM_006710635.2:c.3632-11C>T	XP_006710698.1:n.3632-11C>T
XM_011541429.1:c.3632-11C>T	XP_011539731.1:n.3632-11C>T
XM_011541430.1:c.2759-11C>T	XP_011539732.1:n.2759-11C>T
XM_011541431.1:c.1898-11C>T	XP_011539733.1:n.1898-11C>T
XR_946650.1:n.3699-11C>T
NM_001364727.1:c.3317-11C>T	NP_001351656.1:n.3317-11C>T
XM_005244749.3:c.3632-11C>T	XP_005244806.1:n.3632-11C>T
XM_011541429.2:c.3632-11C>T	XP_011539731.1:n.3632-11C>T
XR_946650.2:n.3703-11C>T
NM_001305275.2:c.3632-11C>T	NP_001292204.1:n.3632-11C>T
NM_198576.4:c.3632-11C>T MANE Select	NP_940978.2:n.3632-11C>T
NM_001364727.2:c.3317-11C>T	NP_001351656.1:n.3317-11C>T