Canonical Allele Identifier: CA337812169

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.957608A>C (hg19) ; chr1:g.1022228A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022228A>C , CM000663.2:g.1022228A>C	GRCh38
NC_000001.10:g.957608A>C , CM000663.1:g.957608A>C	GRCh37
NC_000001.9:g.947471A>C	NCBI36
NG_016346.1:g.7106A>C , LRG_198:g.7106A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379370.7:c.229A>C MANE Select	ENSP00000368678.2:p.Lys77Gln
ENST00000379370.6:c.229A>C	ENSP00000368678.2:p.Lys77Gln
ENST00000620552.4:c.-186A>C	ENSP00000484607.1:n.-186A>C
NM_001305275.1:c.229A>C	NP_001292204.1:p.Lys77Gln
NM_198576.3:c.229A>C	NP_940978.2:p.Lys77Gln
XM_005244749.2:c.229A>C	XP_005244806.1:p.Lys77Gln
XM_006710635.2:c.229A>C	XP_006710698.1:p.Lys77Gln
XM_011541429.1:c.229A>C	XP_011539731.1:p.Lys77Gln
XM_011541430.1:c.229A>C	XP_011539732.1:p.Lys77Gln
XR_946650.1:n.296A>C
XM_005244749.3:c.229A>C	XP_005244806.1:p.Lys77Gln
XM_011541429.2:c.229A>C	XP_011539731.1:p.Lys77Gln
XR_946650.2:n.300A>C
NM_001305275.2:c.229A>C	NP_001292204.1:p.Lys77Gln
NM_198576.4:c.229A>C MANE Select	NP_940978.2:p.Lys77Gln