Canonical Allele Identifier: CA2642497226
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1049868_1049887del , CM000663.2:g.1049868_1049887del GRCh38
NC_000001.10:g.985248_985267del , CM000663.1:g.985248_985267del GRCh37
NC_000001.9:g.975111_975130del NCBI36
NG_016346.1:g.34746_34765del , LRG_198:g.34746_34765del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4745-35_4745-16del MANE Select ENSP00000368678.2:n.4745-35_4745-16del
ENST00000651234.1:c.4430-35_4430-16del ENSP00000499046.1:n.4430-35_4430-16del
ENST00000652369.1:c.4430-35_4430-16del ENSP00000498543.1:n.4430-35_4430-16del
ENST00000379370.6:c.4745-35_4745-16del ENSP00000368678.2:n.4745-35_4745-16del
ENST00000620552.4:c.4331-35_4331-16del ENSP00000484607.1:n.4331-35_4331-16del
NM_001305275.1:c.4745-35_4745-16del NP_001292204.1:n.4745-35_4745-16del
NM_198576.3:c.4745-35_4745-16del NP_940978.2:n.4745-35_4745-16del
XM_005244749.2:c.4745-35_4745-16del XP_005244806.1:n.4745-35_4745-16del
XM_006710635.2:c.4745-35_4745-16del XP_006710698.1:n.4745-35_4745-16del
XM_011541429.1:c.4745-35_4745-16del XP_011539731.1:n.4745-35_4745-16del
XM_011541430.1:c.3872-35_3872-16del XP_011539732.1:n.3872-35_3872-16del
XM_011541431.1:c.3011-35_3011-16del XP_011539733.1:n.3011-35_3011-16del
XR_946650.1:n.4812-35_4812-16del
NM_001364727.1:c.4430-35_4430-16del NP_001351656.1:n.4430-35_4430-16del
XM_005244749.3:c.4745-35_4745-16del XP_005244806.1:n.4745-35_4745-16del
XM_011541429.2:c.4745-35_4745-16del XP_011539731.1:n.4745-35_4745-16del
XR_946650.2:n.4816-35_4816-16del
NM_001305275.2:c.4745-35_4745-16del NP_001292204.1:n.4745-35_4745-16del
NM_198576.4:c.4745-35_4745-16del MANE Select NP_940978.2:n.4745-35_4745-16del
NM_001364727.2:c.4430-35_4430-16del NP_001351656.1:n.4430-35_4430-16del