Canonical Allele Identifier: CA966955

Gene: AGL

Linked Data

• ClinVar Variation Id: 2059501
• ClinVar RCV Id: RCV002952833
• dbSNP Id: rs756310563
• ExAC: 1:100357260 C / T
• gnomAD v2: 1-100357260-C-T
• gnomAD v3: 1-99891704-C-T
• gnomAD v4: 1-99891704-C-T
• MyVariant Identifiers: chr1:g.100357260C>T (hg19) ; chr1:g.99891704C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99891704C>T , CM000663.2:g.99891704C>T	GRCh38
NC_000001.10:g.100357260C>T , CM000663.1:g.100357260C>T	GRCh37
NC_000001.9:g.100129848C>T	NCBI36
NG_012865.1:g.46621C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3048C>T MANE Select	ENSP00000355106.3:p.Thr1016=
ENST00000637337.1:n.3259C>T
ENST00000294724.8:c.3048C>T	ENSP00000294724.4:p.Thr1016=
ENST00000361302.7:c.3000C>T	ENSP00000354971.3:p.Thr1000=
ENST00000361522.4:c.2997C>T	ENSP00000354635.4:p.Thr999=
ENST00000361915.7:c.3048C>T	ENSP00000355106.3:p.Thr1016=
ENST00000370161.6:c.3000C>T	ENSP00000359180.2:p.Thr1000=
ENST00000370163.7:c.3048C>T	ENSP00000359182.3:p.Thr1016=
ENST00000370165.7:c.3048C>T	ENSP00000359184.3:p.Thr1016=
NM_000028.2:c.3048C>T	NP_000019.2:p.Thr1016=
NM_000642.2:c.3048C>T	NP_000633.2:p.Thr1016=
NM_000643.2:c.3048C>T	NP_000634.2:p.Thr1016=
NM_000644.2:c.3048C>T	NP_000635.2:p.Thr1016=
NM_000645.2:c.2997C>T	NP_000636.2:p.Thr999=
NM_000646.2:c.3000C>T	NP_000637.2:p.Thr1000=
XM_005270557.1:c.3048C>T	XP_005270614.1:p.Thr1016=
XM_005270557.2:c.3048C>T	XP_005270614.1:p.Thr1016=
XM_017000501.2:c.1308C>T	XP_016855990.1:p.Thr436=
NM_000642.3:c.3048C>T MANE Select	NP_000633.2:p.Thr1016=