Canonical Allele Identifier: CA645621485

Gene: AGRN

Linked Data

• COSMIC: COSN22818554

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049855_1049868del , CM000663.2:g.1049855_1049868del	GRCh38
NC_000001.10:g.985235_985248del , CM000663.1:g.985235_985248del	GRCh37
NC_000001.9:g.975098_975111del	NCBI36
NG_016346.1:g.34733_34746del , LRG_198:g.34733_34746del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4745-48_4745-35del MANE Select	ENSP00000368678.2:n.4745-48_4745-35del
ENST00000651234.1:c.4430-48_4430-35del	ENSP00000499046.1:n.4430-48_4430-35del
ENST00000652369.1:c.4430-48_4430-35del	ENSP00000498543.1:n.4430-48_4430-35del
ENST00000379370.6:c.4745-48_4745-35del	ENSP00000368678.2:n.4745-48_4745-35del
ENST00000620552.4:c.4331-48_4331-35del	ENSP00000484607.1:n.4331-48_4331-35del
NM_001305275.1:c.4745-48_4745-35del	NP_001292204.1:n.4745-48_4745-35del
NM_198576.3:c.4745-48_4745-35del	NP_940978.2:n.4745-48_4745-35del
XM_005244749.2:c.4745-48_4745-35del	XP_005244806.1:n.4745-48_4745-35del
XM_006710635.2:c.4745-48_4745-35del	XP_006710698.1:n.4745-48_4745-35del
XM_011541429.1:c.4745-48_4745-35del	XP_011539731.1:n.4745-48_4745-35del
XM_011541430.1:c.3872-48_3872-35del	XP_011539732.1:n.3872-48_3872-35del
XM_011541431.1:c.3011-48_3011-35del	XP_011539733.1:n.3011-48_3011-35del
XR_946650.1:n.4812-48_4812-35del
NM_001364727.1:c.4430-48_4430-35del	NP_001351656.1:n.4430-48_4430-35del
XM_005244749.3:c.4745-48_4745-35del	XP_005244806.1:n.4745-48_4745-35del
XM_011541429.2:c.4745-48_4745-35del	XP_011539731.1:n.4745-48_4745-35del
XR_946650.2:n.4816-48_4816-35del
NM_001305275.2:c.4745-48_4745-35del	NP_001292204.1:n.4745-48_4745-35del
NM_198576.4:c.4745-48_4745-35del MANE Select	NP_940978.2:n.4745-48_4745-35del
NM_001364727.2:c.4430-48_4430-35del	NP_001351656.1:n.4430-48_4430-35del