Canonical Allele Identifier: CA419096419

Gene: AGL

Linked Data

• ClinVar Variation Id: 1549630
• ClinVar RCV Id: RCV002182826
• dbSNP Id: rs2101112216
• MyVariant Identifiers: chr1:g.100336029T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99870473T>C , CM000663.2:g.99870473T>C	GRCh38
NC_000001.10:g.100336029T>C , CM000663.1:g.100336029T>C	GRCh37
NC_000001.9:g.100108617T>C	NCBI36
NG_012865.1:g.25390T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.738T>C MANE Select	ENSP00000355106.3:p.Pro246=
ENST00000637337.1:n.949T>C
ENST00000294724.8:c.738T>C	ENSP00000294724.4:p.Pro246=
ENST00000361302.7:c.690T>C	ENSP00000354971.3:p.Pro230=
ENST00000361522.4:c.687T>C	ENSP00000354635.4:p.Pro229=
ENST00000361915.7:c.738T>C	ENSP00000355106.3:p.Pro246=
ENST00000370161.6:c.690T>C	ENSP00000359180.2:p.Pro230=
ENST00000370163.7:c.738T>C	ENSP00000359182.3:p.Pro246=
ENST00000370165.7:c.738T>C	ENSP00000359184.3:p.Pro246=
NM_000028.2:c.738T>C	NP_000019.2:p.Pro246=
NM_000642.2:c.738T>C	NP_000633.2:p.Pro246=
NM_000643.2:c.738T>C	NP_000634.2:p.Pro246=
NM_000644.2:c.738T>C	NP_000635.2:p.Pro246=
NM_000645.2:c.687T>C	NP_000636.2:p.Pro229=
NM_000646.2:c.690T>C	NP_000637.2:p.Pro230=
XM_005270557.1:c.738T>C	XP_005270614.1:p.Pro246=
XM_005270557.2:c.738T>C	XP_005270614.1:p.Pro246=
NM_000642.3:c.738T>C MANE Select	NP_000633.2:p.Pro246=