Canonical Allele Identifier: CA16760091

Gene: AGRN

Linked Data

• dbSNP Id: rs969431985
• gnomAD v4: 1-1047981-A-T
• MyVariant Identifiers: chr1:g.983361A>T (hg19) ; chr1:g.1047981A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047981A>T , CM000663.2:g.1047981A>T	GRCh38
NC_000001.10:g.983361A>T , CM000663.1:g.983361A>T	GRCh37
NC_000001.9:g.973224A>T	NCBI36
NG_016346.1:g.32859A>T , LRG_198:g.32859A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3752-31A>T MANE Select	ENSP00000368678.2:n.3752-31A>T
ENST00000651234.1:c.3437-31A>T	ENSP00000499046.1:n.3437-31A>T
ENST00000652369.1:c.3437-31A>T	ENSP00000498543.1:n.3437-31A>T
ENST00000379370.6:c.3752-31A>T	ENSP00000368678.2:n.3752-31A>T
ENST00000620552.4:c.3338-31A>T	ENSP00000484607.1:n.3338-31A>T
NM_001305275.1:c.3752-31A>T	NP_001292204.1:n.3752-31A>T
NM_198576.3:c.3752-31A>T	NP_940978.2:n.3752-31A>T
XM_005244749.2:c.3752-31A>T	XP_005244806.1:n.3752-31A>T
XM_006710635.2:c.3752-31A>T	XP_006710698.1:n.3752-31A>T
XM_011541429.1:c.3752-31A>T	XP_011539731.1:n.3752-31A>T
XM_011541430.1:c.2879-31A>T	XP_011539732.1:n.2879-31A>T
XM_011541431.1:c.2018-31A>T	XP_011539733.1:n.2018-31A>T
XR_946650.1:n.3819-31A>T
NM_001364727.1:c.3437-31A>T	NP_001351656.1:n.3437-31A>T
XM_005244749.3:c.3752-31A>T	XP_005244806.1:n.3752-31A>T
XM_011541429.2:c.3752-31A>T	XP_011539731.1:n.3752-31A>T
XR_946650.2:n.3823-31A>T
NM_001305275.2:c.3752-31A>T	NP_001292204.1:n.3752-31A>T
NM_198576.4:c.3752-31A>T MANE Select	NP_940978.2:n.3752-31A>T
NM_001364727.2:c.3437-31A>T	NP_001351656.1:n.3437-31A>T