Canonical Allele Identifier: CA337852949

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983539A>C (hg19) ; chr1:g.1048159A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048159A>C , CM000663.2:g.1048159A>C	GRCh38
NC_000001.10:g.983539A>C , CM000663.1:g.983539A>C	GRCh37
NC_000001.9:g.973402A>C	NCBI36
NG_016346.1:g.33037A>C , LRG_198:g.33037A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3899A>C MANE Select	ENSP00000368678.2:p.Lys1300Thr
ENST00000651234.1:c.3584A>C	ENSP00000499046.1:p.Lys1195Thr
ENST00000652369.1:c.3584A>C	ENSP00000498543.1:p.Lys1195Thr
ENST00000379370.6:c.3899A>C	ENSP00000368678.2:p.Lys1300Thr
ENST00000620552.4:c.3485A>C	ENSP00000484607.1:p.Lys1162Thr
NM_001305275.1:c.3899A>C	NP_001292204.1:p.Lys1300Thr
NM_198576.3:c.3899A>C	NP_940978.2:p.Lys1300Thr
XM_005244749.2:c.3899A>C	XP_005244806.1:p.Lys1300Thr
XM_006710635.2:c.3899A>C	XP_006710698.1:p.Lys1300Thr
XM_011541429.1:c.3899A>C	XP_011539731.1:p.Lys1300Thr
XM_011541430.1:c.3026A>C	XP_011539732.1:p.Lys1009Thr
XM_011541431.1:c.2165A>C	XP_011539733.1:p.Lys722Thr
XR_946650.1:n.3966A>C
NM_001364727.1:c.3584A>C	NP_001351656.1:p.Lys1195Thr
XM_005244749.3:c.3899A>C	XP_005244806.1:p.Lys1300Thr
XM_011541429.2:c.3899A>C	XP_011539731.1:p.Lys1300Thr
XR_946650.2:n.3970A>C
NM_001305275.2:c.3899A>C	NP_001292204.1:p.Lys1300Thr
NM_198576.4:c.3899A>C MANE Select	NP_940978.2:p.Lys1300Thr
NM_001364727.2:c.3584A>C	NP_001351656.1:p.Lys1195Thr