Canonical Allele Identifier: CA1148773902

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044059_1044061delinsCTG , CM000663.2:g.1044059_1044061delinsCTG	GRCh38
NC_000001.10:g.979439_979441delinsCTG , CM000663.1:g.979439_979441delinsCTG	GRCh37
NC_000001.9:g.969302_969304delinsCTG	NCBI36
NG_016346.1:g.28937_28939delinsCTG , LRG_198:g.28937_28939delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1999+36_1999+38delinsCTG MANE Select	ENSP00000368678.2:n.1999+36_1999+38delinsCTG
ENST00000651234.1:c.1684+36_1684+38delinsCTG	ENSP00000499046.1:n.1684+36_1684+38delinsCTG
ENST00000652369.1:c.1684+36_1684+38delinsCTG	ENSP00000498543.1:n.1684+36_1684+38delinsCTG
ENST00000379370.6:c.1999+36_1999+38delinsCTG	ENSP00000368678.2:n.1999+36_1999+38delinsCTG
ENST00000620552.4:c.1585+36_1585+38delinsCTG	ENSP00000484607.1:n.1585+36_1585+38delinsCTG
NM_001305275.1:c.1999+36_1999+38delinsCTG	NP_001292204.1:n.1999+36_1999+38delinsCTG
NM_198576.3:c.1999+36_1999+38delinsCTG	NP_940978.2:n.1999+36_1999+38delinsCTG
XM_005244749.2:c.1999+36_1999+38delinsCTG	XP_005244806.1:n.1999+36_1999+38delinsCTG
XM_006710635.2:c.1999+36_1999+38delinsCTG	XP_006710698.1:n.1999+36_1999+38delinsCTG
XM_011541429.1:c.1999+36_1999+38delinsCTG	XP_011539731.1:n.1999+36_1999+38delinsCTG
XM_011541430.1:c.1126+36_1126+38delinsCTG	XP_011539732.1:n.1126+36_1126+38delinsCTG
XM_011541431.1:c.265+36_265+38delinsCTG	XP_011539733.1:n.265+36_265+38delinsCTG
XR_946650.1:n.2066+36_2066+38delinsCTG
NM_001364727.1:c.1684+36_1684+38delinsCTG	NP_001351656.1:n.1684+36_1684+38delinsCTG
XM_005244749.3:c.1999+36_1999+38delinsCTG	XP_005244806.1:n.1999+36_1999+38delinsCTG
XM_011541429.2:c.1999+36_1999+38delinsCTG	XP_011539731.1:n.1999+36_1999+38delinsCTG
XR_946650.2:n.2070+36_2070+38delinsCTG
NM_001305275.2:c.1999+36_1999+38delinsCTG	NP_001292204.1:n.1999+36_1999+38delinsCTG
NM_198576.4:c.1999+36_1999+38delinsCTG MANE Select	NP_940978.2:n.1999+36_1999+38delinsCTG
NM_001364727.2:c.1684+36_1684+38delinsCTG	NP_001351656.1:n.1684+36_1684+38delinsCTG