Canonical Allele Identifier: CA337852343

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983434T>C (hg19) ; chr1:g.1048054T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048054T>C , CM000663.2:g.1048054T>C	GRCh38
NC_000001.10:g.983434T>C , CM000663.1:g.983434T>C	GRCh37
NC_000001.9:g.973297T>C	NCBI36
NG_016346.1:g.32932T>C , LRG_198:g.32932T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3794T>C MANE Select	ENSP00000368678.2:p.Ile1265Thr
ENST00000651234.1:c.3479T>C	ENSP00000499046.1:p.Ile1160Thr
ENST00000652369.1:c.3479T>C	ENSP00000498543.1:p.Ile1160Thr
ENST00000379370.6:c.3794T>C	ENSP00000368678.2:p.Ile1265Thr
ENST00000620552.4:c.3380T>C	ENSP00000484607.1:p.Ile1127Thr
NM_001305275.1:c.3794T>C	NP_001292204.1:p.Ile1265Thr
NM_198576.3:c.3794T>C	NP_940978.2:p.Ile1265Thr
XM_005244749.2:c.3794T>C	XP_005244806.1:p.Ile1265Thr
XM_006710635.2:c.3794T>C	XP_006710698.1:p.Ile1265Thr
XM_011541429.1:c.3794T>C	XP_011539731.1:p.Ile1265Thr
XM_011541430.1:c.2921T>C	XP_011539732.1:p.Ile974Thr
XM_011541431.1:c.2060T>C	XP_011539733.1:p.Ile687Thr
XR_946650.1:n.3861T>C
NM_001364727.1:c.3479T>C	NP_001351656.1:p.Ile1160Thr
XM_005244749.3:c.3794T>C	XP_005244806.1:p.Ile1265Thr
XM_011541429.2:c.3794T>C	XP_011539731.1:p.Ile1265Thr
XR_946650.2:n.3865T>C
NM_001305275.2:c.3794T>C	NP_001292204.1:p.Ile1265Thr
NM_198576.4:c.3794T>C MANE Select	NP_940978.2:p.Ile1265Thr
NM_001364727.2:c.3479T>C	NP_001351656.1:p.Ile1160Thr