Canonical Allele Identifier: CA337779439

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985342C>A (hg19) ; chr1:g.1049962C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049962C>A , CM000663.2:g.1049962C>A	GRCh38
NC_000001.10:g.985342C>A , CM000663.1:g.985342C>A	GRCh37
NC_000001.9:g.975205C>A	NCBI36
NG_016346.1:g.34840C>A , LRG_198:g.34840C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4804C>A MANE Select	ENSP00000368678.2:p.Pro1602Thr
ENST00000651234.1:c.4489C>A	ENSP00000499046.1:p.Pro1497Thr
ENST00000652369.1:c.4489C>A	ENSP00000498543.1:p.Pro1497Thr
ENST00000379370.6:c.4804C>A	ENSP00000368678.2:p.Pro1602Thr
ENST00000620552.4:c.4390C>A	ENSP00000484607.1:p.Pro1464Thr
NM_001305275.1:c.4804C>A	NP_001292204.1:p.Pro1602Thr
NM_198576.3:c.4804C>A	NP_940978.2:p.Pro1602Thr
XM_005244749.2:c.4804C>A	XP_005244806.1:p.Pro1602Thr
XM_006710635.2:c.4804C>A	XP_006710698.1:p.Pro1602Thr
XM_011541429.1:c.4804C>A	XP_011539731.1:p.Pro1602Thr
XM_011541430.1:c.3931C>A	XP_011539732.1:p.Pro1311Thr
XM_011541431.1:c.3070C>A	XP_011539733.1:p.Pro1024Thr
XR_946650.1:n.4871C>A
NM_001364727.1:c.4489C>A	NP_001351656.1:p.Pro1497Thr
XM_005244749.3:c.4804C>A	XP_005244806.1:p.Pro1602Thr
XM_011541429.2:c.4804C>A	XP_011539731.1:p.Pro1602Thr
XR_946650.2:n.4875C>A
NM_001305275.2:c.4804C>A	NP_001292204.1:p.Pro1602Thr
NM_198576.4:c.4804C>A MANE Select	NP_940978.2:p.Pro1602Thr
NM_001364727.2:c.4489C>A	NP_001351656.1:p.Pro1497Thr