Canonical Allele Identifier: CA337852162

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983399T>A (hg19) ; chr1:g.1048019T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048019T>A , CM000663.2:g.1048019T>A	GRCh38
NC_000001.10:g.983399T>A , CM000663.1:g.983399T>A	GRCh37
NC_000001.9:g.973262T>A	NCBI36
NG_016346.1:g.32897T>A , LRG_198:g.32897T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3759T>A MANE Select	ENSP00000368678.2:p.Phe1253Leu
ENST00000651234.1:c.3444T>A	ENSP00000499046.1:p.Phe1148Leu
ENST00000652369.1:c.3444T>A	ENSP00000498543.1:p.Phe1148Leu
ENST00000379370.6:c.3759T>A	ENSP00000368678.2:p.Phe1253Leu
ENST00000620552.4:c.3345T>A	ENSP00000484607.1:p.Phe1115Leu
NM_001305275.1:c.3759T>A	NP_001292204.1:p.Phe1253Leu
NM_198576.3:c.3759T>A	NP_940978.2:p.Phe1253Leu
XM_005244749.2:c.3759T>A	XP_005244806.1:p.Phe1253Leu
XM_006710635.2:c.3759T>A	XP_006710698.1:p.Phe1253Leu
XM_011541429.1:c.3759T>A	XP_011539731.1:p.Phe1253Leu
XM_011541430.1:c.2886T>A	XP_011539732.1:p.Phe962Leu
XM_011541431.1:c.2025T>A	XP_011539733.1:p.Phe675Leu
XR_946650.1:n.3826T>A
NM_001364727.1:c.3444T>A	NP_001351656.1:p.Phe1148Leu
XM_005244749.3:c.3759T>A	XP_005244806.1:p.Phe1253Leu
XM_011541429.2:c.3759T>A	XP_011539731.1:p.Phe1253Leu
XR_946650.2:n.3830T>A
NM_001305275.2:c.3759T>A	NP_001292204.1:p.Phe1253Leu
NM_198576.4:c.3759T>A MANE Select	NP_940978.2:p.Phe1253Leu
NM_001364727.2:c.3444T>A	NP_001351656.1:p.Phe1148Leu