Canonical Allele Identifier: CA1148751185

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050518_1050521delinsTTCG , CM000663.2:g.1050518_1050521delinsTTCG	GRCh38
NC_000001.10:g.985898_985901delinsTTCG , CM000663.1:g.985898_985901delinsTTCG	GRCh37
NC_000001.9:g.975761_975764delinsTTCG	NCBI36
NG_016346.1:g.35396_35399delinsTTCG , LRG_198:g.35396_35399delinsTTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.5068_5071delinsTTCG MANE Select	ENSP00000368678.2:p.Phe1690=
ENST00000651234.1:c.4753_4756delinsTTCG	ENSP00000499046.1:p.Phe1585=
ENST00000652369.1:c.4753_4756delinsTTCG	ENSP00000498543.1:p.Phe1585=
ENST00000379370.6:c.5068_5071delinsTTCG	ENSP00000368678.2:p.Phe1690=
ENST00000620552.4:c.4654_4657delinsTTCG	ENSP00000484607.1:p.Phe1552=
NM_001305275.1:c.5068_5071delinsTTCG	NP_001292204.1:p.Phe1690=
NM_198576.3:c.5068_5071delinsTTCG	NP_940978.2:p.Phe1690=
XM_005244749.2:c.5068_5071delinsTTCG	XP_005244806.1:p.Phe1690=
XM_006710635.2:c.5068_5071delinsTTCG	XP_006710698.1:p.Phe1690=
XM_011541429.1:c.5068_5071delinsTTCG	XP_011539731.1:p.Phe1690=
XM_011541430.1:c.4195_4198delinsTTCG	XP_011539732.1:p.Phe1399=
XM_011541431.1:c.3334_3337delinsTTCG	XP_011539733.1:p.Phe1112=
XR_946650.1:n.5135_5138delinsTTCG
NM_001364727.1:c.4753_4756delinsTTCG	NP_001351656.1:p.Phe1585=
XM_005244749.3:c.5068_5071delinsTTCG	XP_005244806.1:p.Phe1690=
XM_011541429.2:c.5068_5071delinsTTCG	XP_011539731.1:p.Phe1690=
XR_946650.2:n.5139_5142delinsTTCG
NM_001305275.2:c.5068_5071delinsTTCG	NP_001292204.1:p.Phe1690=
NM_198576.4:c.5068_5071delinsTTCG MANE Select	NP_940978.2:p.Phe1690=
NM_001364727.2:c.4753_4756delinsTTCG	NP_001351656.1:p.Phe1585=