Canonical Allele Identifier: CA337812232

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.957614C>G (hg19) ; chr1:g.1022234C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022234C>G , CM000663.2:g.1022234C>G	GRCh38
NC_000001.10:g.957614C>G , CM000663.1:g.957614C>G	GRCh37
NC_000001.9:g.947477C>G	NCBI36
NG_016346.1:g.7112C>G , LRG_198:g.7112C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000379370.7:c.235C>G MANE Select	ENSP00000368678.2:p.Leu79Val
ENST00000379370.6:c.235C>G	ENSP00000368678.2:p.Leu79Val
ENST00000620552.4:c.-180C>G	ENSP00000484607.1:n.-180C>G
NM_001305275.1:c.235C>G	NP_001292204.1:p.Leu79Val
NM_198576.3:c.235C>G	NP_940978.2:p.Leu79Val
XM_005244749.2:c.235C>G	XP_005244806.1:p.Leu79Val
XM_006710635.2:c.235C>G	XP_006710698.1:p.Leu79Val
XM_011541429.1:c.235C>G	XP_011539731.1:p.Leu79Val
XM_011541430.1:c.235C>G	XP_011539732.1:p.Leu79Val
XR_946650.1:n.302C>G
XM_005244749.3:c.235C>G	XP_005244806.1:p.Leu79Val
XM_011541429.2:c.235C>G	XP_011539731.1:p.Leu79Val
XR_946650.2:n.306C>G
NM_001305275.2:c.235C>G	NP_001292204.1:p.Leu79Val
NM_198576.4:c.235C>G MANE Select	NP_940978.2:p.Leu79Val