Canonical Allele Identifier: CA337853027

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983557C>G (hg19) ; chr1:g.1048177C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048177C>G , CM000663.2:g.1048177C>G	GRCh38
NC_000001.10:g.983557C>G , CM000663.1:g.983557C>G	GRCh37
NC_000001.9:g.973420C>G	NCBI36
NG_016346.1:g.33055C>G , LRG_198:g.33055C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3917C>G MANE Select	ENSP00000368678.2:p.Thr1306Ser
ENST00000651234.1:c.3602C>G	ENSP00000499046.1:p.Thr1201Ser
ENST00000652369.1:c.3602C>G	ENSP00000498543.1:p.Thr1201Ser
ENST00000379370.6:c.3917C>G	ENSP00000368678.2:p.Thr1306Ser
ENST00000620552.4:c.3503C>G	ENSP00000484607.1:p.Thr1168Ser
NM_001305275.1:c.3917C>G	NP_001292204.1:p.Thr1306Ser
NM_198576.3:c.3917C>G	NP_940978.2:p.Thr1306Ser
XM_005244749.2:c.3917C>G	XP_005244806.1:p.Thr1306Ser
XM_006710635.2:c.3917C>G	XP_006710698.1:p.Thr1306Ser
XM_011541429.1:c.3917C>G	XP_011539731.1:p.Thr1306Ser
XM_011541430.1:c.3044C>G	XP_011539732.1:p.Thr1015Ser
XM_011541431.1:c.2183C>G	XP_011539733.1:p.Thr728Ser
XR_946650.1:n.3984C>G
NM_001364727.1:c.3602C>G	NP_001351656.1:p.Thr1201Ser
XM_005244749.3:c.3917C>G	XP_005244806.1:p.Thr1306Ser
XM_011541429.2:c.3917C>G	XP_011539731.1:p.Thr1306Ser
XR_946650.2:n.3988C>G
NM_001305275.2:c.3917C>G	NP_001292204.1:p.Thr1306Ser
NM_198576.4:c.3917C>G MANE Select	NP_940978.2:p.Thr1306Ser
NM_001364727.2:c.3602C>G	NP_001351656.1:p.Thr1201Ser