Canonical Allele Identifier: CA341343381

Gene: AGL

Linked Data

• ClinVar Variation Id: 2674803
• ClinVar RCV Id: RCV003466165
• MyVariant Identifiers: chr1:g.100387098G>A (hg19) ; chr1:g.99921542G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921542G>A , CM000663.2:g.99921542G>A	GRCh38
NC_000001.10:g.100387098G>A , CM000663.1:g.100387098G>A	GRCh37
NC_000001.9:g.100159686G>A	NCBI36
NG_012865.1:g.76459G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4490G>A MANE Select	ENSP00000355106.3:p.Trp1497Ter
ENST00000637337.1:n.4701G>A
ENST00000294724.8:c.4490G>A	ENSP00000294724.4:p.Trp1497Ter
ENST00000361302.7:c.4442G>A	ENSP00000354971.3:p.Trp1481Ter
ENST00000361522.4:c.4439G>A	ENSP00000354635.4:p.Trp1480Ter
ENST00000361915.7:c.4490G>A	ENSP00000355106.3:p.Trp1497Ter
ENST00000370161.6:c.4442G>A	ENSP00000359180.2:p.Trp1481Ter
ENST00000370163.7:c.4490G>A	ENSP00000359182.3:p.Trp1497Ter
ENST00000370165.7:c.4490G>A	ENSP00000359184.3:p.Trp1497Ter
NM_000028.2:c.4490G>A	NP_000019.2:p.Trp1497Ter
NM_000642.2:c.4490G>A	NP_000633.2:p.Trp1497Ter
NM_000643.2:c.4490G>A	NP_000634.2:p.Trp1497Ter
NM_000644.2:c.4490G>A	NP_000635.2:p.Trp1497Ter
NM_000645.2:c.4439G>A	NP_000636.2:p.Trp1480Ter
NM_000646.2:c.4442G>A	NP_000637.2:p.Trp1481Ter
XM_005270557.1:c.4490G>A	XP_005270614.1:p.Trp1497Ter
XR_947626.1:n.1317+2696C>T
XR_947627.1:n.1206+2696C>T
XR_947628.1:n.1311+2696C>T
XR_947630.1:n.1249+2696C>T
XR_947632.1:n.1135+2696C>T
XR_947633.1:n.1246+2696C>T
XR_947634.1:n.660+2696C>T
XR_947635.1:n.728+2696C>T
XM_005270557.2:c.4490G>A	XP_005270614.1:p.Trp1497Ter
XM_017000501.2:c.2750G>A	XP_016855990.1:p.Trp917Ter
NM_000642.3:c.4490G>A MANE Select	NP_000633.2:p.Trp1497Ter