Canonical Allele Identifier: CA2573132631

Gene: AGL

Linked Data

• ClinVar Variation Id: 1452488
• ClinVar RCV Id: RCV001999833
• dbSNP Id: rs2101128055

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99875246del , CM000663.2:g.99875246del	GRCh38
NC_000001.10:g.100340802del , CM000663.1:g.100340802del	GRCh37
NC_000001.9:g.100113390del	NCBI36
NG_012865.1:g.30163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1175del MANE Select	ENSP00000355106.3:p.His392LeufsTer25
ENST00000637337.1:n.1386del
ENST00000294724.8:c.1175del	ENSP00000294724.4:p.His392LeufsTer25
ENST00000361302.7:c.1127del	ENSP00000354971.3:p.His376LeufsTer25
ENST00000361522.4:c.1124del	ENSP00000354635.4:p.His375LeufsTer25
ENST00000361915.7:c.1175del	ENSP00000355106.3:p.His392LeufsTer25
ENST00000370161.6:c.1127del	ENSP00000359180.2:p.His376LeufsTer25
ENST00000370163.7:c.1175del	ENSP00000359182.3:p.His392LeufsTer25
ENST00000370165.7:c.1175del	ENSP00000359184.3:p.His392LeufsTer25
ENST00000477753.1:n.434del
NM_000028.2:c.1175del	NP_000019.2:p.His392LeufsTer25
NM_000642.2:c.1175del	NP_000633.2:p.His392LeufsTer25
NM_000643.2:c.1175del	NP_000634.2:p.His392LeufsTer25
NM_000644.2:c.1175del	NP_000635.2:p.His392LeufsTer25
NM_000645.2:c.1124del	NP_000636.2:p.His375LeufsTer25
NM_000646.2:c.1127del	NP_000637.2:p.His376LeufsTer25
XM_005270557.1:c.1175del	XP_005270614.1:p.His392LeufsTer25
XM_005270557.2:c.1175del	XP_005270614.1:p.His392LeufsTer25
NM_000642.3:c.1175del MANE Select	NP_000633.2:p.His392LeufsTer25