Canonical Allele Identifier: CA1148773734

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044030_1044031delinsCG , CM000663.2:g.1044030_1044031delinsCG	GRCh38
NC_000001.10:g.979410_979411delinsCG , CM000663.1:g.979410_979411delinsCG	GRCh37
NC_000001.9:g.969273_969274delinsCG	NCBI36
NG_016346.1:g.28908_28909delinsCG , LRG_198:g.28908_28909delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1999+7_1999+8delinsCG MANE Select	ENSP00000368678.2:n.1999+7_1999+8delinsCG
ENST00000651234.1:c.1684+7_1684+8delinsCG	ENSP00000499046.1:n.1684+7_1684+8delinsCG
ENST00000652369.1:c.1684+7_1684+8delinsCG	ENSP00000498543.1:n.1684+7_1684+8delinsCG
ENST00000379370.6:c.1999+7_1999+8delinsCG	ENSP00000368678.2:n.1999+7_1999+8delinsCG
ENST00000620552.4:c.1585+7_1585+8delinsCG	ENSP00000484607.1:n.1585+7_1585+8delinsCG
NM_001305275.1:c.1999+7_1999+8delinsCG	NP_001292204.1:n.1999+7_1999+8delinsCG
NM_198576.3:c.1999+7_1999+8delinsCG	NP_940978.2:n.1999+7_1999+8delinsCG
XM_005244749.2:c.1999+7_1999+8delinsCG	XP_005244806.1:n.1999+7_1999+8delinsCG
XM_006710635.2:c.1999+7_1999+8delinsCG	XP_006710698.1:n.1999+7_1999+8delinsCG
XM_011541429.1:c.1999+7_1999+8delinsCG	XP_011539731.1:n.1999+7_1999+8delinsCG
XM_011541430.1:c.1126+7_1126+8delinsCG	XP_011539732.1:n.1126+7_1126+8delinsCG
XM_011541431.1:c.265+7_265+8delinsCG	XP_011539733.1:n.265+7_265+8delinsCG
XR_946650.1:n.2066+7_2066+8delinsCG
NM_001364727.1:c.1684+7_1684+8delinsCG	NP_001351656.1:n.1684+7_1684+8delinsCG
XM_005244749.3:c.1999+7_1999+8delinsCG	XP_005244806.1:n.1999+7_1999+8delinsCG
XM_011541429.2:c.1999+7_1999+8delinsCG	XP_011539731.1:n.1999+7_1999+8delinsCG
XR_946650.2:n.2070+7_2070+8delinsCG
NM_001305275.2:c.1999+7_1999+8delinsCG	NP_001292204.1:n.1999+7_1999+8delinsCG
NM_198576.4:c.1999+7_1999+8delinsCG MANE Select	NP_940978.2:n.1999+7_1999+8delinsCG
NM_001364727.2:c.1684+7_1684+8delinsCG	NP_001351656.1:n.1684+7_1684+8delinsCG