Canonical Allele Identifier: CA415758042

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983235G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047855G>C , CM000663.2:g.1047855G>C	GRCh38
NC_000001.10:g.983235G>C , CM000663.1:g.983235G>C	GRCh37
NC_000001.9:g.973098G>C	NCBI36
NG_016346.1:g.32733G>C , LRG_198:g.32733G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3711G>C MANE Select	ENSP00000368678.2:p.Val1237=
ENST00000651234.1:c.3396G>C	ENSP00000499046.1:p.Val1132=
ENST00000652369.1:c.3396G>C	ENSP00000498543.1:p.Val1132=
ENST00000379370.6:c.3711G>C	ENSP00000368678.2:p.Val1237=
ENST00000466223.1:n.449G>C
ENST00000620552.4:c.3297G>C	ENSP00000484607.1:p.Val1099=
NM_001305275.1:c.3711G>C	NP_001292204.1:p.Val1237=
NM_198576.3:c.3711G>C	NP_940978.2:p.Val1237=
XM_005244749.2:c.3711G>C	XP_005244806.1:p.Val1237=
XM_006710635.2:c.3711G>C	XP_006710698.1:p.Val1237=
XM_011541429.1:c.3711G>C	XP_011539731.1:p.Val1237=
XM_011541430.1:c.2838G>C	XP_011539732.1:p.Val946=
XM_011541431.1:c.1977G>C	XP_011539733.1:p.Val659=
XR_946650.1:n.3778G>C
NM_001364727.1:c.3396G>C	NP_001351656.1:p.Val1132=
XM_005244749.3:c.3711G>C	XP_005244806.1:p.Val1237=
XM_011541429.2:c.3711G>C	XP_011539731.1:p.Val1237=
XR_946650.2:n.3782G>C
NM_001305275.2:c.3711G>C	NP_001292204.1:p.Val1237=
NM_198576.4:c.3711G>C MANE Select	NP_940978.2:p.Val1237=
NM_001364727.2:c.3396G>C	NP_001351656.1:p.Val1132=