Canonical Allele Identifier: CA337853019

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983556A>T (hg19) ; chr1:g.1048176A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048176A>T , CM000663.2:g.1048176A>T	GRCh38
NC_000001.10:g.983556A>T , CM000663.1:g.983556A>T	GRCh37
NC_000001.9:g.973419A>T	NCBI36
NG_016346.1:g.33054A>T , LRG_198:g.33054A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3916A>T MANE Select	ENSP00000368678.2:p.Thr1306Ser
ENST00000651234.1:c.3601A>T	ENSP00000499046.1:p.Thr1201Ser
ENST00000652369.1:c.3601A>T	ENSP00000498543.1:p.Thr1201Ser
ENST00000379370.6:c.3916A>T	ENSP00000368678.2:p.Thr1306Ser
ENST00000620552.4:c.3502A>T	ENSP00000484607.1:p.Thr1168Ser
NM_001305275.1:c.3916A>T	NP_001292204.1:p.Thr1306Ser
NM_198576.3:c.3916A>T	NP_940978.2:p.Thr1306Ser
XM_005244749.2:c.3916A>T	XP_005244806.1:p.Thr1306Ser
XM_006710635.2:c.3916A>T	XP_006710698.1:p.Thr1306Ser
XM_011541429.1:c.3916A>T	XP_011539731.1:p.Thr1306Ser
XM_011541430.1:c.3043A>T	XP_011539732.1:p.Thr1015Ser
XM_011541431.1:c.2182A>T	XP_011539733.1:p.Thr728Ser
XR_946650.1:n.3983A>T
NM_001364727.1:c.3601A>T	NP_001351656.1:p.Thr1201Ser
XM_005244749.3:c.3916A>T	XP_005244806.1:p.Thr1306Ser
XM_011541429.2:c.3916A>T	XP_011539731.1:p.Thr1306Ser
XR_946650.2:n.3987A>T
NM_001305275.2:c.3916A>T	NP_001292204.1:p.Thr1306Ser
NM_198576.4:c.3916A>T MANE Select	NP_940978.2:p.Thr1306Ser
NM_001364727.2:c.3601A>T	NP_001351656.1:p.Thr1201Ser