Canonical Allele Identifier: CA337853282

Gene: AGRN

Linked Data

• gnomAD v4: 1-1048263-T-C
• MyVariant Identifiers: chr1:g.983643T>C (hg19) ; chr1:g.1048263T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048263T>C , CM000663.2:g.1048263T>C	GRCh38
NC_000001.10:g.983643T>C , CM000663.1:g.983643T>C	GRCh37
NC_000001.9:g.973506T>C	NCBI36
NG_016346.1:g.33141T>C , LRG_198:g.33141T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4003T>C MANE Select	ENSP00000368678.2:p.Ser1335Pro
ENST00000651234.1:c.3688T>C	ENSP00000499046.1:p.Ser1230Pro
ENST00000652369.1:c.3688T>C	ENSP00000498543.1:p.Ser1230Pro
ENST00000379370.6:c.4003T>C	ENSP00000368678.2:p.Ser1335Pro
ENST00000620552.4:c.3589T>C	ENSP00000484607.1:p.Ser1197Pro
NM_001305275.1:c.4003T>C	NP_001292204.1:p.Ser1335Pro
NM_198576.3:c.4003T>C	NP_940978.2:p.Ser1335Pro
XM_005244749.2:c.4003T>C	XP_005244806.1:p.Ser1335Pro
XM_006710635.2:c.4003T>C	XP_006710698.1:p.Ser1335Pro
XM_011541429.1:c.4003T>C	XP_011539731.1:p.Ser1335Pro
XM_011541430.1:c.3130T>C	XP_011539732.1:p.Ser1044Pro
XM_011541431.1:c.2269T>C	XP_011539733.1:p.Ser757Pro
XR_946650.1:n.4070T>C
NM_001364727.1:c.3688T>C	NP_001351656.1:p.Ser1230Pro
XM_005244749.3:c.4003T>C	XP_005244806.1:p.Ser1335Pro
XM_011541429.2:c.4003T>C	XP_011539731.1:p.Ser1335Pro
XR_946650.2:n.4074T>C
NM_001305275.2:c.4003T>C	NP_001292204.1:p.Ser1335Pro
NM_198576.4:c.4003T>C MANE Select	NP_940978.2:p.Ser1335Pro
NM_001364727.2:c.3688T>C	NP_001351656.1:p.Ser1230Pro