Canonical Allele Identifier: CA337851128

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983156C>A (hg19) ; chr1:g.1047776C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047776C>A , CM000663.2:g.1047776C>A	GRCh38
NC_000001.10:g.983156C>A , CM000663.1:g.983156C>A	GRCh37
NC_000001.9:g.973019C>A	NCBI36
NG_016346.1:g.32654C>A , LRG_198:g.32654C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3632C>A MANE Select	ENSP00000368678.2:p.Thr1211Asn
ENST00000651234.1:c.3317C>A	ENSP00000499046.1:p.Thr1106Asn
ENST00000652369.1:c.3317C>A	ENSP00000498543.1:p.Thr1106Asn
ENST00000379370.6:c.3632C>A	ENSP00000368678.2:p.Thr1211Asn
ENST00000466223.1:n.370C>A
ENST00000478677.1:n.214C>A
ENST00000620552.4:c.3218C>A	ENSP00000484607.1:p.Thr1073Asn
NM_001305275.1:c.3632C>A	NP_001292204.1:p.Thr1211Asn
NM_198576.3:c.3632C>A	NP_940978.2:p.Thr1211Asn
XM_005244749.2:c.3632C>A	XP_005244806.1:p.Thr1211Asn
XM_006710635.2:c.3632C>A	XP_006710698.1:p.Thr1211Asn
XM_011541429.1:c.3632C>A	XP_011539731.1:p.Thr1211Asn
XM_011541430.1:c.2759C>A	XP_011539732.1:p.Thr920Asn
XM_011541431.1:c.1898C>A	XP_011539733.1:p.Thr633Asn
XR_946650.1:n.3699C>A
NM_001364727.1:c.3317C>A	NP_001351656.1:p.Thr1106Asn
XM_005244749.3:c.3632C>A	XP_005244806.1:p.Thr1211Asn
XM_011541429.2:c.3632C>A	XP_011539731.1:p.Thr1211Asn
XR_946650.2:n.3703C>A
NM_001305275.2:c.3632C>A	NP_001292204.1:p.Thr1211Asn
NM_198576.4:c.3632C>A MANE Select	NP_940978.2:p.Thr1211Asn
NM_001364727.2:c.3317C>A	NP_001351656.1:p.Thr1106Asn