Canonical Allele Identifier: CA419097249

Gene: AGL

Linked Data

• MyVariant Identifiers: chr1:g.100342077A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99876521A>T , CM000663.2:g.99876521A>T	GRCh38
NC_000001.10:g.100342077A>T , CM000663.1:g.100342077A>T	GRCh37
NC_000001.9:g.100114665A>T	NCBI36
NG_012865.1:g.31438A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1347A>T MANE Select	ENSP00000355106.3:p.Pro449=
ENST00000637337.1:n.1558A>T
ENST00000294724.8:c.1347A>T	ENSP00000294724.4:p.Pro449=
ENST00000361302.7:c.1299A>T	ENSP00000354971.3:p.Pro433=
ENST00000361522.4:c.1296A>T	ENSP00000354635.4:p.Pro432=
ENST00000361915.7:c.1347A>T	ENSP00000355106.3:p.Pro449=
ENST00000370161.6:c.1299A>T	ENSP00000359180.2:p.Pro433=
ENST00000370163.7:c.1347A>T	ENSP00000359182.3:p.Pro449=
ENST00000370165.7:c.1347A>T	ENSP00000359184.3:p.Pro449=
ENST00000477753.1:n.606A>T
NM_000028.2:c.1347A>T	NP_000019.2:p.Pro449=
NM_000642.2:c.1347A>T	NP_000633.2:p.Pro449=
NM_000643.2:c.1347A>T	NP_000634.2:p.Pro449=
NM_000644.2:c.1347A>T	NP_000635.2:p.Pro449=
NM_000645.2:c.1296A>T	NP_000636.2:p.Pro432=
NM_000646.2:c.1299A>T	NP_000637.2:p.Pro433=
XM_005270557.1:c.1347A>T	XP_005270614.1:p.Pro449=
XM_005270557.2:c.1347A>T	XP_005270614.1:p.Pro449=
NM_000642.3:c.1347A>T MANE Select	NP_000633.2:p.Pro449=