Canonical Allele Identifier: CA419095332

Gene: AGL

Linked Data

• ClinVar Variation Id: 1577205
• ClinVar RCV Id: RCV002080851
• dbSNP Id: rs2101087013
• gnomAD v4: 1-99862287-T-C
• MyVariant Identifiers: chr1:g.100327843T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99862287T>C , CM000663.2:g.99862287T>C	GRCh38
NC_000001.10:g.100327843T>C , CM000663.1:g.100327843T>C	GRCh37
NC_000001.9:g.100100431T>C	NCBI36
NG_012865.1:g.17204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.324T>C MANE Select	ENSP00000355106.3:p.Val108=
ENST00000637337.1:n.535T>C
ENST00000294724.8:c.324T>C	ENSP00000294724.4:p.Val108=
ENST00000361302.7:c.276T>C	ENSP00000354971.3:p.Val92=
ENST00000361522.4:c.273T>C	ENSP00000354635.4:p.Val91=
ENST00000361915.7:c.324T>C	ENSP00000355106.3:p.Val108=
ENST00000370161.6:c.276T>C	ENSP00000359180.2:p.Val92=
ENST00000370163.7:c.324T>C	ENSP00000359182.3:p.Val108=
ENST00000370165.7:c.324T>C	ENSP00000359184.3:p.Val108=
NM_000028.2:c.324T>C	NP_000019.2:p.Val108=
NM_000642.2:c.324T>C	NP_000633.2:p.Val108=
NM_000643.2:c.324T>C	NP_000634.2:p.Val108=
NM_000644.2:c.324T>C	NP_000635.2:p.Val108=
NM_000645.2:c.273T>C	NP_000636.2:p.Val91=
NM_000646.2:c.276T>C	NP_000637.2:p.Val92=
XM_005270557.1:c.324T>C	XP_005270614.1:p.Val108=
XM_005270557.2:c.324T>C	XP_005270614.1:p.Val108=
NM_000642.3:c.324T>C MANE Select	NP_000633.2:p.Val108=