Canonical Allele Identifier: CA2742134870

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047688_1047775del , CM000663.2:g.1047688_1047775del	GRCh38
NC_000001.10:g.983068_983155del , CM000663.1:g.983068_983155del	GRCh37
NC_000001.9:g.972931_973018del	NCBI36
NG_016346.1:g.32566_32653del , LRG_198:g.32566_32653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3631+1_3632-1del MANE Select	ENSP00000368678.2:n.3631+1_3632-1del
ENST00000651234.1:c.3316+1_3317-1del	ENSP00000499046.1:n.3316+1_3317-1del
ENST00000652369.1:c.3316+1_3317-1del	ENSP00000498543.1:n.3316+1_3317-1del
ENST00000379370.6:c.3631+1_3632-1del	ENSP00000368678.2:n.3631+1_3632-1del
ENST00000466223.1:n.369+1_370-1del
ENST00000478677.1:n.213+1_214-1del
ENST00000620552.4:c.3217+1_3218-1del	ENSP00000484607.1:n.3217+1_3218-1del
NM_001305275.1:c.3631+1_3632-1del	NP_001292204.1:n.3631+1_3632-1del
NM_198576.3:c.3631+1_3632-1del	NP_940978.2:n.3631+1_3632-1del
XM_005244749.2:c.3631+1_3632-1del	XP_005244806.1:n.3631+1_3632-1del
XM_006710635.2:c.3631+1_3632-1del	XP_006710698.1:n.3631+1_3632-1del
XM_011541429.1:c.3631+1_3632-1del	XP_011539731.1:n.3631+1_3632-1del
XM_011541430.1:c.2758+1_2759-1del	XP_011539732.1:n.2758+1_2759-1del
XM_011541431.1:c.1897+1_1898-1del	XP_011539733.1:n.1897+1_1898-1del
XR_946650.1:n.3698+1_3699-1del
NM_001364727.1:c.3316+1_3317-1del	NP_001351656.1:n.3316+1_3317-1del
XM_005244749.3:c.3631+1_3632-1del	XP_005244806.1:n.3631+1_3632-1del
XM_011541429.2:c.3631+1_3632-1del	XP_011539731.1:n.3631+1_3632-1del
XR_946650.2:n.3702+1_3703-1del
NM_001305275.2:c.3631+1_3632-1del	NP_001292204.1:n.3631+1_3632-1del
NM_198576.4:c.3631+1_3632-1del MANE Select	NP_940978.2:n.3631+1_3632-1del
NM_001364727.2:c.3316+1_3317-1del	NP_001351656.1:n.3316+1_3317-1del