Canonical Allele Identifier: CA337779468

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985357C>T (hg19) ; chr1:g.1049977C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049977C>T , CM000663.2:g.1049977C>T	GRCh38
NC_000001.10:g.985357C>T , CM000663.1:g.985357C>T	GRCh37
NC_000001.9:g.975220C>T	NCBI36
NG_016346.1:g.34855C>T , LRG_198:g.34855C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379370.7:c.4819C>T MANE Select	ENSP00000368678.2:p.Pro1607Ser
ENST00000651234.1:c.4504C>T	ENSP00000499046.1:p.Pro1502Ser
ENST00000652369.1:c.4504C>T	ENSP00000498543.1:p.Pro1502Ser
ENST00000379370.6:c.4819C>T	ENSP00000368678.2:p.Pro1607Ser
ENST00000620552.4:c.4405C>T	ENSP00000484607.1:p.Pro1469Ser
NM_001305275.1:c.4819C>T	NP_001292204.1:p.Pro1607Ser
NM_198576.3:c.4819C>T	NP_940978.2:p.Pro1607Ser
XM_005244749.2:c.4819C>T	XP_005244806.1:p.Pro1607Ser
XM_006710635.2:c.4819C>T	XP_006710698.1:p.Pro1607Ser
XM_011541429.1:c.4819C>T	XP_011539731.1:p.Pro1607Ser
XM_011541430.1:c.3946C>T	XP_011539732.1:p.Pro1316Ser
XM_011541431.1:c.3085C>T	XP_011539733.1:p.Pro1029Ser
XR_946650.1:n.4886C>T
NM_001364727.1:c.4504C>T	NP_001351656.1:p.Pro1502Ser
XM_005244749.3:c.4819C>T	XP_005244806.1:p.Pro1607Ser
XM_011541429.2:c.4819C>T	XP_011539731.1:p.Pro1607Ser
XR_946650.2:n.4890C>T
NM_001305275.2:c.4819C>T	NP_001292204.1:p.Pro1607Ser
NM_198576.4:c.4819C>T MANE Select	NP_940978.2:p.Pro1607Ser
NM_001364727.2:c.4504C>T	NP_001351656.1:p.Pro1502Ser