Canonical Allele Identifier: CA415756907

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.979228T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043848T>C , CM000663.2:g.1043848T>C	GRCh38
NC_000001.10:g.979228T>C , CM000663.1:g.979228T>C	GRCh37
NC_000001.9:g.969091T>C	NCBI36
NG_016346.1:g.28726T>C , LRG_198:g.28726T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1824T>C MANE Select	ENSP00000368678.2:p.Ala608=
ENST00000651234.1:c.1509T>C	ENSP00000499046.1:p.Ala503=
ENST00000652369.1:c.1509T>C	ENSP00000498543.1:p.Ala503=
ENST00000379370.6:c.1824T>C	ENSP00000368678.2:p.Ala608=
ENST00000620552.4:c.1410T>C	ENSP00000484607.1:p.Ala470=
NM_001305275.1:c.1824T>C	NP_001292204.1:p.Ala608=
NM_198576.3:c.1824T>C	NP_940978.2:p.Ala608=
XM_005244749.2:c.1824T>C	XP_005244806.1:p.Ala608=
XM_006710635.2:c.1824T>C	XP_006710698.1:p.Ala608=
XM_011541429.1:c.1824T>C	XP_011539731.1:p.Ala608=
XM_011541430.1:c.951T>C	XP_011539732.1:p.Ala317=
XM_011541431.1:c.90T>C	XP_011539733.1:p.Ala30=
XR_946650.1:n.1891T>C
NM_001364727.1:c.1509T>C	NP_001351656.1:p.Ala503=
XM_005244749.3:c.1824T>C	XP_005244806.1:p.Ala608=
XM_011541429.2:c.1824T>C	XP_011539731.1:p.Ala608=
XR_946650.2:n.1895T>C
NM_001305275.2:c.1824T>C	NP_001292204.1:p.Ala608=
NM_198576.4:c.1824T>C MANE Select	NP_940978.2:p.Ala608=
NM_001364727.2:c.1509T>C	NP_001351656.1:p.Ala503=