Canonical Allele Identifier: CA337780060

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985875A>C (hg19) ; chr1:g.1050495A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050495A>C , CM000663.2:g.1050495A>C	GRCh38
NC_000001.10:g.985875A>C , CM000663.1:g.985875A>C	GRCh37
NC_000001.9:g.975738A>C	NCBI36
NG_016346.1:g.35373A>C , LRG_198:g.35373A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.5045A>C MANE Select	ENSP00000368678.2:p.Gln1682Pro
ENST00000651234.1:c.4730A>C	ENSP00000499046.1:p.Gln1577Pro
ENST00000652369.1:c.4730A>C	ENSP00000498543.1:p.Gln1577Pro
ENST00000379370.6:c.5045A>C	ENSP00000368678.2:p.Gln1682Pro
ENST00000620552.4:c.4631A>C	ENSP00000484607.1:p.Gln1544Pro
NM_001305275.1:c.5045A>C	NP_001292204.1:p.Gln1682Pro
NM_198576.3:c.5045A>C	NP_940978.2:p.Gln1682Pro
XM_005244749.2:c.5045A>C	XP_005244806.1:p.Gln1682Pro
XM_006710635.2:c.5045A>C	XP_006710698.1:p.Gln1682Pro
XM_011541429.1:c.5045A>C	XP_011539731.1:p.Gln1682Pro
XM_011541430.1:c.4172A>C	XP_011539732.1:p.Gln1391Pro
XM_011541431.1:c.3311A>C	XP_011539733.1:p.Gln1104Pro
XR_946650.1:n.5112A>C
NM_001364727.1:c.4730A>C	NP_001351656.1:p.Gln1577Pro
XM_005244749.3:c.5045A>C	XP_005244806.1:p.Gln1682Pro
XM_011541429.2:c.5045A>C	XP_011539731.1:p.Gln1682Pro
XR_946650.2:n.5116A>C
NM_001305275.2:c.5045A>C	NP_001292204.1:p.Gln1682Pro
NM_198576.4:c.5045A>C MANE Select	NP_940978.2:p.Gln1682Pro
NM_001364727.2:c.4730A>C	NP_001351656.1:p.Gln1577Pro