Canonical Allele Identifier: CA415758482

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983684A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048304A>C , CM000663.2:g.1048304A>C	GRCh38
NC_000001.10:g.983684A>C , CM000663.1:g.983684A>C	GRCh37
NC_000001.9:g.973547A>C	NCBI36
NG_016346.1:g.33182A>C , LRG_198:g.33182A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4044A>C MANE Select	ENSP00000368678.2:p.Ala1348=
ENST00000651234.1:c.3729A>C	ENSP00000499046.1:p.Ala1243=
ENST00000652369.1:c.3729A>C	ENSP00000498543.1:p.Ala1243=
ENST00000379370.6:c.4044A>C	ENSP00000368678.2:p.Ala1348=
ENST00000620552.4:c.3630A>C	ENSP00000484607.1:p.Ala1210=
NM_001305275.1:c.4044A>C	NP_001292204.1:p.Ala1348=
NM_198576.3:c.4044A>C	NP_940978.2:p.Ala1348=
XM_005244749.2:c.4044A>C	XP_005244806.1:p.Ala1348=
XM_006710635.2:c.4044A>C	XP_006710698.1:p.Ala1348=
XM_011541429.1:c.4044A>C	XP_011539731.1:p.Ala1348=
XM_011541430.1:c.3171A>C	XP_011539732.1:p.Ala1057=
XM_011541431.1:c.2310A>C	XP_011539733.1:p.Ala770=
XR_946650.1:n.4111A>C
NM_001364727.1:c.3729A>C	NP_001351656.1:p.Ala1243=
XM_005244749.3:c.4044A>C	XP_005244806.1:p.Ala1348=
XM_011541429.2:c.4044A>C	XP_011539731.1:p.Ala1348=
XR_946650.2:n.4115A>C
NM_001305275.2:c.4044A>C	NP_001292204.1:p.Ala1348=
NM_198576.4:c.4044A>C MANE Select	NP_940978.2:p.Ala1348=
NM_001364727.2:c.3729A>C	NP_001351656.1:p.Ala1243=