Canonical Allele Identifier: CA1148805163

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048249_1048251delinsCAA , CM000663.2:g.1048249_1048251delinsCAA	GRCh38
NC_000001.10:g.983629_983631delinsCAA , CM000663.1:g.983629_983631delinsCAA	GRCh37
NC_000001.9:g.973492_973494delinsCAA	NCBI36
NG_016346.1:g.33127_33129delinsCAA , LRG_198:g.33127_33129delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3989_3991delinsCAA MANE Select	ENSP00000368678.2:p.Pro1330=
ENST00000651234.1:c.3674_3676delinsCAA	ENSP00000499046.1:p.Pro1225=
ENST00000652369.1:c.3674_3676delinsCAA	ENSP00000498543.1:p.Pro1225=
ENST00000379370.6:c.3989_3991delinsCAA	ENSP00000368678.2:p.Pro1330=
ENST00000620552.4:c.3575_3577delinsCAA	ENSP00000484607.1:p.Pro1192=
NM_001305275.1:c.3989_3991delinsCAA	NP_001292204.1:p.Pro1330=
NM_198576.3:c.3989_3991delinsCAA	NP_940978.2:p.Pro1330=
XM_005244749.2:c.3989_3991delinsCAA	XP_005244806.1:p.Pro1330=
XM_006710635.2:c.3989_3991delinsCAA	XP_006710698.1:p.Pro1330=
XM_011541429.1:c.3989_3991delinsCAA	XP_011539731.1:p.Pro1330=
XM_011541430.1:c.3116_3118delinsCAA	XP_011539732.1:p.Pro1039=
XM_011541431.1:c.2255_2257delinsCAA	XP_011539733.1:p.Pro752=
XR_946650.1:n.4056_4058delinsCAA
NM_001364727.1:c.3674_3676delinsCAA	NP_001351656.1:p.Pro1225=
XM_005244749.3:c.3989_3991delinsCAA	XP_005244806.1:p.Pro1330=
XM_011541429.2:c.3989_3991delinsCAA	XP_011539731.1:p.Pro1330=
XR_946650.2:n.4060_4062delinsCAA
NM_001305275.2:c.3989_3991delinsCAA	NP_001292204.1:p.Pro1330=
NM_198576.4:c.3989_3991delinsCAA MANE Select	NP_940978.2:p.Pro1330=
NM_001364727.2:c.3674_3676delinsCAA	NP_001351656.1:p.Pro1225=