Canonical Allele Identifier: CA337851499

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983228T>G (hg19) ; chr1:g.1047848T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047848T>G , CM000663.2:g.1047848T>G	GRCh38
NC_000001.10:g.983228T>G , CM000663.1:g.983228T>G	GRCh37
NC_000001.9:g.973091T>G	NCBI36
NG_016346.1:g.32726T>G , LRG_198:g.32726T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3704T>G MANE Select	ENSP00000368678.2:p.Leu1235Trp
ENST00000651234.1:c.3389T>G	ENSP00000499046.1:p.Leu1130Trp
ENST00000652369.1:c.3389T>G	ENSP00000498543.1:p.Leu1130Trp
ENST00000379370.6:c.3704T>G	ENSP00000368678.2:p.Leu1235Trp
ENST00000466223.1:n.442T>G
ENST00000620552.4:c.3290T>G	ENSP00000484607.1:p.Leu1097Trp
NM_001305275.1:c.3704T>G	NP_001292204.1:p.Leu1235Trp
NM_198576.3:c.3704T>G	NP_940978.2:p.Leu1235Trp
XM_005244749.2:c.3704T>G	XP_005244806.1:p.Leu1235Trp
XM_006710635.2:c.3704T>G	XP_006710698.1:p.Leu1235Trp
XM_011541429.1:c.3704T>G	XP_011539731.1:p.Leu1235Trp
XM_011541430.1:c.2831T>G	XP_011539732.1:p.Leu944Trp
XM_011541431.1:c.1970T>G	XP_011539733.1:p.Leu657Trp
XR_946650.1:n.3771T>G
NM_001364727.1:c.3389T>G	NP_001351656.1:p.Leu1130Trp
XM_005244749.3:c.3704T>G	XP_005244806.1:p.Leu1235Trp
XM_011541429.2:c.3704T>G	XP_011539731.1:p.Leu1235Trp
XR_946650.2:n.3775T>G
NM_001305275.2:c.3704T>G	NP_001292204.1:p.Leu1235Trp
NM_198576.4:c.3704T>G MANE Select	NP_940978.2:p.Leu1235Trp
NM_001364727.2:c.3389T>G	NP_001351656.1:p.Leu1130Trp