Canonical Allele Identifier: CA1148773443

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043999_1044000delinsGC , CM000663.2:g.1043999_1044000delinsGC	GRCh38
NC_000001.10:g.979379_979380delinsGC , CM000663.1:g.979379_979380delinsGC	GRCh37
NC_000001.9:g.969242_969243delinsGC	NCBI36
NG_016346.1:g.28877_28878delinsGC , LRG_198:g.28877_28878delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1975_1976delinsGC MANE Select	ENSP00000368678.2:p.Ala659=
ENST00000651234.1:c.1660_1661delinsGC	ENSP00000499046.1:p.Ala554=
ENST00000652369.1:c.1660_1661delinsGC	ENSP00000498543.1:p.Ala554=
ENST00000379370.6:c.1975_1976delinsGC	ENSP00000368678.2:p.Ala659=
ENST00000620552.4:c.1561_1562delinsGC	ENSP00000484607.1:p.Ala521=
NM_001305275.1:c.1975_1976delinsGC	NP_001292204.1:p.Ala659=
NM_198576.3:c.1975_1976delinsGC	NP_940978.2:p.Ala659=
XM_005244749.2:c.1975_1976delinsGC	XP_005244806.1:p.Ala659=
XM_006710635.2:c.1975_1976delinsGC	XP_006710698.1:p.Ala659=
XM_011541429.1:c.1975_1976delinsGC	XP_011539731.1:p.Ala659=
XM_011541430.1:c.1102_1103delinsGC	XP_011539732.1:p.Ala368=
XM_011541431.1:c.241_242delinsGC	XP_011539733.1:p.Ala81=
XR_946650.1:n.2042_2043delinsGC
NM_001364727.1:c.1660_1661delinsGC	NP_001351656.1:p.Ala554=
XM_005244749.3:c.1975_1976delinsGC	XP_005244806.1:p.Ala659=
XM_011541429.2:c.1975_1976delinsGC	XP_011539731.1:p.Ala659=
XR_946650.2:n.2046_2047delinsGC
NM_001305275.2:c.1975_1976delinsGC	NP_001292204.1:p.Ala659=
NM_198576.4:c.1975_1976delinsGC MANE Select	NP_940978.2:p.Ala659=
NM_001364727.2:c.1660_1661delinsGC	NP_001351656.1:p.Ala554=