Canonical Allele Identifier: CA27550826

Gene: AGL

Linked Data

• ClinVar Variation Id: 2061718
• ClinVar RCV Id: RCV002952891
• dbSNP Id: rs781592803
• gnomAD v2: 1-100316674-G-C
• gnomAD v4: 1-99851118-G-C
• MyVariant Identifiers: chr1:g.100316674G>C (hg19) ; chr1:g.99851118G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99851118G>C , CM000663.2:g.99851118G>C	GRCh38
NC_000001.10:g.100316674G>C , CM000663.1:g.100316674G>C	GRCh37
NC_000001.9:g.100089262G>C	NCBI36
NG_012865.1:g.6035G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.76G>C MANE Select	ENSP00000355106.3:p.Glu26Gln
ENST00000294724.8:c.76G>C	ENSP00000294724.4:p.Glu26Gln
ENST00000361302.7:c.-116G>C	ENSP00000354971.3:n.-116G>C
ENST00000361915.7:c.76G>C	ENSP00000355106.3:p.Glu26Gln
ENST00000370163.7:c.76G>C	ENSP00000359182.3:p.Glu26Gln
ENST00000370165.7:c.76G>C	ENSP00000359184.3:p.Glu26Gln
NM_000028.2:c.76G>C	NP_000019.2:p.Glu26Gln
NM_000642.2:c.76G>C	NP_000633.2:p.Glu26Gln
NM_000643.2:c.76G>C	NP_000634.2:p.Glu26Gln
NM_000644.2:c.76G>C	NP_000635.2:p.Glu26Gln
NM_000646.2:c.-116G>C	NP_000637.2:n.-116G>C
XM_005270557.1:c.76G>C	XP_005270614.1:p.Glu26Gln
XM_005270557.2:c.76G>C	XP_005270614.1:p.Glu26Gln
NM_000642.3:c.76G>C MANE Select	NP_000633.2:p.Glu26Gln