Canonical Allele Identifier: CA1183924661

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99862466_99862467delinsTG , CM000663.2:g.99862466_99862467delinsTG	GRCh38
NC_000001.10:g.100328022_100328023delinsTG , CM000663.1:g.100328022_100328023delinsTG	GRCh37
NC_000001.9:g.100100610_100100611delinsTG	NCBI36
NG_012865.1:g.17383_17384delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.460+43_460+44delinsTG MANE Select	ENSP00000355106.3:n.460+43_460+44delinsTG
ENST00000637337.1:n.671+43_671+44delinsTG
ENST00000294724.8:c.460+43_460+44delinsTG	ENSP00000294724.4:n.460+43_460+44delinsTG
ENST00000361302.7:c.412+43_412+44delinsTG	ENSP00000354971.3:n.412+43_412+44delinsTG
ENST00000361522.4:c.409+43_409+44delinsTG	ENSP00000354635.4:n.409+43_409+44delinsTG
ENST00000361915.7:c.460+43_460+44delinsTG	ENSP00000355106.3:n.460+43_460+44delinsTG
ENST00000370161.6:c.412+43_412+44delinsTG	ENSP00000359180.2:n.412+43_412+44delinsTG
ENST00000370163.7:c.460+43_460+44delinsTG	ENSP00000359182.3:n.460+43_460+44delinsTG
ENST00000370165.7:c.460+43_460+44delinsTG	ENSP00000359184.3:n.460+43_460+44delinsTG
NM_000028.2:c.460+43_460+44delinsTG	NP_000019.2:n.460+43_460+44delinsTG
NM_000642.2:c.460+43_460+44delinsTG	NP_000633.2:n.460+43_460+44delinsTG
NM_000643.2:c.460+43_460+44delinsTG	NP_000634.2:n.460+43_460+44delinsTG
NM_000644.2:c.460+43_460+44delinsTG	NP_000635.2:n.460+43_460+44delinsTG
NM_000645.2:c.409+43_409+44delinsTG	NP_000636.2:n.409+43_409+44delinsTG
NM_000646.2:c.412+43_412+44delinsTG	NP_000637.2:n.412+43_412+44delinsTG
XM_005270557.1:c.460+43_460+44delinsTG	XP_005270614.1:n.460+43_460+44delinsTG
XM_005270557.2:c.460+43_460+44delinsTG	XP_005270614.1:n.460+43_460+44delinsTG
NM_000642.3:c.460+43_460+44delinsTG MANE Select	NP_000633.2:n.460+43_460+44delinsTG