Canonical Allele Identifier: CA337779995

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985860T>C (hg19) ; chr1:g.1050480T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050480T>C , CM000663.2:g.1050480T>C	GRCh38
NC_000001.10:g.985860T>C , CM000663.1:g.985860T>C	GRCh37
NC_000001.9:g.975723T>C	NCBI36
NG_016346.1:g.35358T>C , LRG_198:g.35358T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379370.7:c.5030T>C MANE Select	ENSP00000368678.2:p.Leu1677Pro
ENST00000651234.1:c.4715T>C	ENSP00000499046.1:p.Leu1572Pro
ENST00000652369.1:c.4715T>C	ENSP00000498543.1:p.Leu1572Pro
ENST00000379370.6:c.5030T>C	ENSP00000368678.2:p.Leu1677Pro
ENST00000620552.4:c.4616T>C	ENSP00000484607.1:p.Leu1539Pro
NM_001305275.1:c.5030T>C	NP_001292204.1:p.Leu1677Pro
NM_198576.3:c.5030T>C	NP_940978.2:p.Leu1677Pro
XM_005244749.2:c.5030T>C	XP_005244806.1:p.Leu1677Pro
XM_006710635.2:c.5030T>C	XP_006710698.1:p.Leu1677Pro
XM_011541429.1:c.5030T>C	XP_011539731.1:p.Leu1677Pro
XM_011541430.1:c.4157T>C	XP_011539732.1:p.Leu1386Pro
XM_011541431.1:c.3296T>C	XP_011539733.1:p.Leu1099Pro
XR_946650.1:n.5097T>C
NM_001364727.1:c.4715T>C	NP_001351656.1:p.Leu1572Pro
XM_005244749.3:c.5030T>C	XP_005244806.1:p.Leu1677Pro
XM_011541429.2:c.5030T>C	XP_011539731.1:p.Leu1677Pro
XR_946650.2:n.5101T>C
NM_001305275.2:c.5030T>C	NP_001292204.1:p.Leu1677Pro
NM_198576.4:c.5030T>C MANE Select	NP_940978.2:p.Leu1677Pro
NM_001364727.2:c.4715T>C	NP_001351656.1:p.Leu1572Pro