Canonical Allele Identifier: CA337836236

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.979593C>T (hg19) ; chr1:g.1044213C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044213C>T , CM000663.2:g.1044213C>T	GRCh38
NC_000001.10:g.979593C>T , CM000663.1:g.979593C>T	GRCh37
NC_000001.9:g.969456C>T	NCBI36
NG_016346.1:g.29091C>T , LRG_198:g.29091C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.2104C>T MANE Select	ENSP00000368678.2:p.Pro702Ser
ENST00000651234.1:c.1789C>T	ENSP00000499046.1:p.Pro597Ser
ENST00000652369.1:c.1789C>T	ENSP00000498543.1:p.Pro597Ser
ENST00000379370.6:c.2104C>T	ENSP00000368678.2:p.Pro702Ser
ENST00000620552.4:c.1690C>T	ENSP00000484607.1:p.Pro564Ser
NM_001305275.1:c.2104C>T	NP_001292204.1:p.Pro702Ser
NM_198576.3:c.2104C>T	NP_940978.2:p.Pro702Ser
XM_005244749.2:c.2104C>T	XP_005244806.1:p.Pro702Ser
XM_006710635.2:c.2104C>T	XP_006710698.1:p.Pro702Ser
XM_011541429.1:c.2104C>T	XP_011539731.1:p.Pro702Ser
XM_011541430.1:c.1231C>T	XP_011539732.1:p.Pro411Ser
XM_011541431.1:c.370C>T	XP_011539733.1:p.Pro124Ser
XR_946650.1:n.2171C>T
NM_001364727.1:c.1789C>T	NP_001351656.1:p.Pro597Ser
XM_005244749.3:c.2104C>T	XP_005244806.1:p.Pro702Ser
XM_011541429.2:c.2104C>T	XP_011539731.1:p.Pro702Ser
XR_946650.2:n.2175C>T
NM_001305275.2:c.2104C>T	NP_001292204.1:p.Pro702Ser
NM_198576.4:c.2104C>T MANE Select	NP_940978.2:p.Pro702Ser
NM_001364727.2:c.1789C>T	NP_001351656.1:p.Pro597Ser