Canonical Allele Identifier: CA337834497

Gene: AGRN

Linked Data

• gnomAD v4: 1-1043858-G-A
• MyVariant Identifiers: chr1:g.979238G>A (hg19) ; chr1:g.1043858G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043858G>A , CM000663.2:g.1043858G>A	GRCh38
NC_000001.10:g.979238G>A , CM000663.1:g.979238G>A	GRCh37
NC_000001.9:g.969101G>A	NCBI36
NG_016346.1:g.28736G>A , LRG_198:g.28736G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1834G>A MANE Select	ENSP00000368678.2:p.Val612Met
ENST00000651234.1:c.1519G>A	ENSP00000499046.1:p.Val507Met
ENST00000652369.1:c.1519G>A	ENSP00000498543.1:p.Val507Met
ENST00000379370.6:c.1834G>A	ENSP00000368678.2:p.Val612Met
ENST00000620552.4:c.1420G>A	ENSP00000484607.1:p.Val474Met
NM_001305275.1:c.1834G>A	NP_001292204.1:p.Val612Met
NM_198576.3:c.1834G>A	NP_940978.2:p.Val612Met
XM_005244749.2:c.1834G>A	XP_005244806.1:p.Val612Met
XM_006710635.2:c.1834G>A	XP_006710698.1:p.Val612Met
XM_011541429.1:c.1834G>A	XP_011539731.1:p.Val612Met
XM_011541430.1:c.961G>A	XP_011539732.1:p.Val321Met
XM_011541431.1:c.100G>A	XP_011539733.1:p.Val34Met
XR_946650.1:n.1901G>A
NM_001364727.1:c.1519G>A	NP_001351656.1:p.Val507Met
XM_005244749.3:c.1834G>A	XP_005244806.1:p.Val612Met
XM_011541429.2:c.1834G>A	XP_011539731.1:p.Val612Met
XR_946650.2:n.1905G>A
NM_001305275.2:c.1834G>A	NP_001292204.1:p.Val612Met
NM_198576.4:c.1834G>A MANE Select	NP_940978.2:p.Val612Met
NM_001364727.2:c.1519G>A	NP_001351656.1:p.Val507Met