Canonical Allele Identifier: CA1183944891

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921572A= , CM000663.2:g.99921572A=	GRCh38
NC_000001.10:g.100387128A= , CM000663.1:g.100387128A=	GRCh37
NC_000001.9:g.100159716A=	NCBI36
NG_012865.1:g.76489A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4520A= MANE Select	ENSP00000355106.3:p.Asn1507=
ENST00000637337.1:n.4731A=
ENST00000294724.8:c.4520A=	ENSP00000294724.4:p.Asn1507=
ENST00000361302.7:c.4472A=	ENSP00000354971.3:p.Asn1491=
ENST00000361522.4:c.4469A=	ENSP00000354635.4:p.Asn1490=
ENST00000361915.7:c.4520A=	ENSP00000355106.3:p.Asn1507=
ENST00000370161.6:c.4472A=	ENSP00000359180.2:p.Asn1491=
ENST00000370163.7:c.4520A=	ENSP00000359182.3:p.Asn1507=
ENST00000370165.7:c.4520A=	ENSP00000359184.3:p.Asn1507=
NM_000028.2:c.4520A=	NP_000019.2:p.Asn1507=
NM_000642.2:c.4520A=	NP_000633.2:p.Asn1507=
NM_000643.2:c.4520A=	NP_000634.2:p.Asn1507=
NM_000644.2:c.4520A=	NP_000635.2:p.Asn1507=
NM_000645.2:c.4469A=	NP_000636.2:p.Asn1490=
NM_000646.2:c.4472A=	NP_000637.2:p.Asn1491=
XM_005270557.1:c.4520A=	XP_005270614.1:p.Asn1507=
XR_947626.1:n.1317+2666T=
XR_947627.1:n.1206+2666T=
XR_947628.1:n.1311+2666T=
XR_947630.1:n.1249+2666T=
XR_947632.1:n.1135+2666T=
XR_947633.1:n.1246+2666T=
XR_947634.1:n.660+2666T=
XR_947635.1:n.728+2666T=
XM_005270557.2:c.4520A=	XP_005270614.1:p.Asn1507=
XM_017000501.2:c.2780A=	XP_016855990.1:p.Asn927=
NM_000642.3:c.4520A= MANE Select	NP_000633.2:p.Asn1507=