Canonical Allele Identifier: CA337812177

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.957609A>T (hg19) ; chr1:g.1022229A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022229A>T , CM000663.2:g.1022229A>T	GRCh38
NC_000001.10:g.957609A>T , CM000663.1:g.957609A>T	GRCh37
NC_000001.9:g.947472A>T	NCBI36
NG_016346.1:g.7107A>T , LRG_198:g.7107A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379370.7:c.230A>T MANE Select	ENSP00000368678.2:p.Lys77Ile
ENST00000379370.6:c.230A>T	ENSP00000368678.2:p.Lys77Ile
ENST00000620552.4:c.-185A>T	ENSP00000484607.1:n.-185A>T
NM_001305275.1:c.230A>T	NP_001292204.1:p.Lys77Ile
NM_198576.3:c.230A>T	NP_940978.2:p.Lys77Ile
XM_005244749.2:c.230A>T	XP_005244806.1:p.Lys77Ile
XM_006710635.2:c.230A>T	XP_006710698.1:p.Lys77Ile
XM_011541429.1:c.230A>T	XP_011539731.1:p.Lys77Ile
XM_011541430.1:c.230A>T	XP_011539732.1:p.Lys77Ile
XR_946650.1:n.297A>T
XM_005244749.3:c.230A>T	XP_005244806.1:p.Lys77Ile
XM_011541429.2:c.230A>T	XP_011539731.1:p.Lys77Ile
XR_946650.2:n.301A>T
NM_001305275.2:c.230A>T	NP_001292204.1:p.Lys77Ile
NM_198576.4:c.230A>T MANE Select	NP_940978.2:p.Lys77Ile