Canonical Allele Identifier: CA1148747179

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049891_1049895delinsTCCTC , CM000663.2:g.1049891_1049895delinsTCCTC	GRCh38
NC_000001.10:g.985271_985275delinsTCCTC , CM000663.1:g.985271_985275delinsTCCTC	GRCh37
NC_000001.9:g.975134_975138delinsTCCTC	NCBI36
NG_016346.1:g.34769_34773delinsTCCTC , LRG_198:g.34769_34773delinsTCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4745-12_4745-8delinsTCCTC MANE Select	ENSP00000368678.2:n.4745-12_4745-8delinsTCCTC
ENST00000651234.1:c.4430-12_4430-8delinsTCCTC	ENSP00000499046.1:n.4430-12_4430-8delinsTCCTC
ENST00000652369.1:c.4430-12_4430-8delinsTCCTC	ENSP00000498543.1:n.4430-12_4430-8delinsTCCTC
ENST00000379370.6:c.4745-12_4745-8delinsTCCTC	ENSP00000368678.2:n.4745-12_4745-8delinsTCCTC
ENST00000620552.4:c.4331-12_4331-8delinsTCCTC	ENSP00000484607.1:n.4331-12_4331-8delinsTCCTC
NM_001305275.1:c.4745-12_4745-8delinsTCCTC	NP_001292204.1:n.4745-12_4745-8delinsTCCTC
NM_198576.3:c.4745-12_4745-8delinsTCCTC	NP_940978.2:n.4745-12_4745-8delinsTCCTC
XM_005244749.2:c.4745-12_4745-8delinsTCCTC	XP_005244806.1:n.4745-12_4745-8delinsTCCTC
XM_006710635.2:c.4745-12_4745-8delinsTCCTC	XP_006710698.1:n.4745-12_4745-8delinsTCCTC
XM_011541429.1:c.4745-12_4745-8delinsTCCTC	XP_011539731.1:n.4745-12_4745-8delinsTCCTC
XM_011541430.1:c.3872-12_3872-8delinsTCCTC	XP_011539732.1:n.3872-12_3872-8delinsTCCTC
XM_011541431.1:c.3011-12_3011-8delinsTCCTC	XP_011539733.1:n.3011-12_3011-8delinsTCCTC
XR_946650.1:n.4812-12_4812-8delinsTCCTC
NM_001364727.1:c.4430-12_4430-8delinsTCCTC	NP_001351656.1:n.4430-12_4430-8delinsTCCTC
XM_005244749.3:c.4745-12_4745-8delinsTCCTC	XP_005244806.1:n.4745-12_4745-8delinsTCCTC
XM_011541429.2:c.4745-12_4745-8delinsTCCTC	XP_011539731.1:n.4745-12_4745-8delinsTCCTC
XR_946650.2:n.4816-12_4816-8delinsTCCTC
NM_001305275.2:c.4745-12_4745-8delinsTCCTC	NP_001292204.1:n.4745-12_4745-8delinsTCCTC
NM_198576.4:c.4745-12_4745-8delinsTCCTC MANE Select	NP_940978.2:n.4745-12_4745-8delinsTCCTC
NM_001364727.2:c.4430-12_4430-8delinsTCCTC	NP_001351656.1:n.4430-12_4430-8delinsTCCTC