Canonical Allele Identifier: CA1148802929

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047939_1047940delinsTG , CM000663.2:g.1047939_1047940delinsTG	GRCh38
NC_000001.10:g.983319_983320delinsTG , CM000663.1:g.983319_983320delinsTG	GRCh37
NC_000001.9:g.973182_973183delinsTG	NCBI36
NG_016346.1:g.32817_32818delinsTG , LRG_198:g.32817_32818delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3751+44_3751+45delinsTG MANE Select	ENSP00000368678.2:n.3751+44_3751+45delinsTG
ENST00000651234.1:c.3436+44_3436+45delinsTG	ENSP00000499046.1:n.3436+44_3436+45delinsTG
ENST00000652369.1:c.3436+44_3436+45delinsTG	ENSP00000498543.1:n.3436+44_3436+45delinsTG
ENST00000379370.6:c.3751+44_3751+45delinsTG	ENSP00000368678.2:n.3751+44_3751+45delinsTG
ENST00000620552.4:c.3337+44_3337+45delinsTG	ENSP00000484607.1:n.3337+44_3337+45delinsTG
NM_001305275.1:c.3751+44_3751+45delinsTG	NP_001292204.1:n.3751+44_3751+45delinsTG
NM_198576.3:c.3751+44_3751+45delinsTG	NP_940978.2:n.3751+44_3751+45delinsTG
XM_005244749.2:c.3751+44_3751+45delinsTG	XP_005244806.1:n.3751+44_3751+45delinsTG
XM_006710635.2:c.3751+44_3751+45delinsTG	XP_006710698.1:n.3751+44_3751+45delinsTG
XM_011541429.1:c.3751+44_3751+45delinsTG	XP_011539731.1:n.3751+44_3751+45delinsTG
XM_011541430.1:c.2878+44_2878+45delinsTG	XP_011539732.1:n.2878+44_2878+45delinsTG
XM_011541431.1:c.2017+44_2017+45delinsTG	XP_011539733.1:n.2017+44_2017+45delinsTG
XR_946650.1:n.3818+44_3818+45delinsTG
NM_001364727.1:c.3436+44_3436+45delinsTG	NP_001351656.1:n.3436+44_3436+45delinsTG
XM_005244749.3:c.3751+44_3751+45delinsTG	XP_005244806.1:n.3751+44_3751+45delinsTG
XM_011541429.2:c.3751+44_3751+45delinsTG	XP_011539731.1:n.3751+44_3751+45delinsTG
XR_946650.2:n.3822+44_3822+45delinsTG
NM_001305275.2:c.3751+44_3751+45delinsTG	NP_001292204.1:n.3751+44_3751+45delinsTG
NM_198576.4:c.3751+44_3751+45delinsTG MANE Select	NP_940978.2:n.3751+44_3751+45delinsTG
NM_001364727.2:c.3436+44_3436+45delinsTG	NP_001351656.1:n.3436+44_3436+45delinsTG