Canonical Allele Identifier: CA10584063

Gene: AGRN

Linked Data

• ClinVar Variation Id: 243037
• ClinVar RCV Id: RCV000235021
• dbSNP Id: rs879253787
• MyVariant Identifiers: chr1:g.957693A>T (hg19) ; chr1:g.1022313A>T (hg38)
• PubMed: PMID:20301347 ; PMID:24951643

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022313A>T , CM000663.2:g.1022313A>T	GRCh38
NC_000001.10:g.957693A>T , CM000663.1:g.957693A>T	GRCh37
NC_000001.9:g.947556A>T	NCBI36
NG_016346.1:g.7191A>T , LRG_198:g.7191A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379370.7:c.314A>T MANE Select	ENSP00000368678.2:p.Asn105Ile
ENST00000379370.6:c.314A>T	ENSP00000368678.2:p.Asn105Ile
ENST00000620552.4:c.-101A>T	ENSP00000484607.1:n.-101A>T
NM_001305275.1:c.314A>T	NP_001292204.1:p.Asn105Ile
NM_198576.3:c.314A>T	NP_940978.2:p.Asn105Ile
XM_005244749.2:c.314A>T	XP_005244806.1:p.Asn105Ile
XM_006710635.2:c.314A>T	XP_006710698.1:p.Asn105Ile
XM_011541429.1:c.314A>T	XP_011539731.1:p.Asn105Ile
XM_011541430.1:c.314A>T	XP_011539732.1:p.Asn105Ile
XR_946650.1:n.381A>T
XM_005244749.3:c.314A>T	XP_005244806.1:p.Asn105Ile
XM_011541429.2:c.314A>T	XP_011539731.1:p.Asn105Ile
XR_946650.2:n.385A>T
NM_001305275.2:c.314A>T	NP_001292204.1:p.Asn105Ile
NM_198576.4:c.314A>T MANE Select	NP_940978.2:p.Asn105Ile