Canonical Allele Identifier: CA337779400

Gene: AGRN

Linked Data

• gnomAD v4: 1-1049942-A-G
• MyVariant Identifiers: chr1:g.985322A>G (hg19) ; chr1:g.1049942A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049942A>G , CM000663.2:g.1049942A>G	GRCh38
NC_000001.10:g.985322A>G , CM000663.1:g.985322A>G	GRCh37
NC_000001.9:g.975185A>G	NCBI36
NG_016346.1:g.34820A>G , LRG_198:g.34820A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4784A>G MANE Select	ENSP00000368678.2:p.Asn1595Ser
ENST00000651234.1:c.4469A>G	ENSP00000499046.1:p.Asn1490Ser
ENST00000652369.1:c.4469A>G	ENSP00000498543.1:p.Asn1490Ser
ENST00000379370.6:c.4784A>G	ENSP00000368678.2:p.Asn1595Ser
ENST00000620552.4:c.4370A>G	ENSP00000484607.1:p.Asn1457Ser
NM_001305275.1:c.4784A>G	NP_001292204.1:p.Asn1595Ser
NM_198576.3:c.4784A>G	NP_940978.2:p.Asn1595Ser
XM_005244749.2:c.4784A>G	XP_005244806.1:p.Asn1595Ser
XM_006710635.2:c.4784A>G	XP_006710698.1:p.Asn1595Ser
XM_011541429.1:c.4784A>G	XP_011539731.1:p.Asn1595Ser
XM_011541430.1:c.3911A>G	XP_011539732.1:p.Asn1304Ser
XM_011541431.1:c.3050A>G	XP_011539733.1:p.Asn1017Ser
XR_946650.1:n.4851A>G
NM_001364727.1:c.4469A>G	NP_001351656.1:p.Asn1490Ser
XM_005244749.3:c.4784A>G	XP_005244806.1:p.Asn1595Ser
XM_011541429.2:c.4784A>G	XP_011539731.1:p.Asn1595Ser
XR_946650.2:n.4855A>G
NM_001305275.2:c.4784A>G	NP_001292204.1:p.Asn1595Ser
NM_198576.4:c.4784A>G MANE Select	NP_940978.2:p.Asn1595Ser
NM_001364727.2:c.4469A>G	NP_001351656.1:p.Asn1490Ser