Canonical Allele Identifier: CA415756303

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.957619G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022239G>T , CM000663.2:g.1022239G>T	GRCh38
NC_000001.10:g.957619G>T , CM000663.1:g.957619G>T	GRCh37
NC_000001.9:g.947482G>T	NCBI36
NG_016346.1:g.7117G>T , LRG_198:g.7117G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379370.7:c.240G>T MANE Select	ENSP00000368678.2:p.Val80=
ENST00000379370.6:c.240G>T	ENSP00000368678.2:p.Val80=
ENST00000620552.4:c.-175G>T	ENSP00000484607.1:n.-175G>T
NM_001305275.1:c.240G>T	NP_001292204.1:p.Val80=
NM_198576.3:c.240G>T	NP_940978.2:p.Val80=
XM_005244749.2:c.240G>T	XP_005244806.1:p.Val80=
XM_006710635.2:c.240G>T	XP_006710698.1:p.Val80=
XM_011541429.1:c.240G>T	XP_011539731.1:p.Val80=
XM_011541430.1:c.240G>T	XP_011539732.1:p.Val80=
XR_946650.1:n.307G>T
XM_005244749.3:c.240G>T	XP_005244806.1:p.Val80=
XM_011541429.2:c.240G>T	XP_011539731.1:p.Val80=
XR_946650.2:n.311G>T
NM_001305275.2:c.240G>T	NP_001292204.1:p.Val80=
NM_198576.4:c.240G>T MANE Select	NP_940978.2:p.Val80=