Canonical Allele Identifier: CA1183926399

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99864395_99864396delinsTG , CM000663.2:g.99864395_99864396delinsTG	GRCh38
NC_000001.10:g.100329951_100329952delinsTG , CM000663.1:g.100329951_100329952delinsTG	GRCh37
NC_000001.9:g.100102539_100102540delinsTG	NCBI36
NG_012865.1:g.19312_19313delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.470_471delinsTG MANE Select	ENSP00000355106.3:p.Met157=
ENST00000637337.1:n.681_682delinsTG
ENST00000294724.8:c.470_471delinsTG	ENSP00000294724.4:p.Met157=
ENST00000361302.7:c.422_423delinsTG	ENSP00000354971.3:p.Met141=
ENST00000361522.4:c.419_420delinsTG	ENSP00000354635.4:p.Met140=
ENST00000361915.7:c.470_471delinsTG	ENSP00000355106.3:p.Met157=
ENST00000370161.6:c.422_423delinsTG	ENSP00000359180.2:p.Met141=
ENST00000370163.7:c.470_471delinsTG	ENSP00000359182.3:p.Met157=
ENST00000370165.7:c.470_471delinsTG	ENSP00000359184.3:p.Met157=
NM_000028.2:c.470_471delinsTG	NP_000019.2:p.Met157=
NM_000642.2:c.470_471delinsTG	NP_000633.2:p.Met157=
NM_000643.2:c.470_471delinsTG	NP_000634.2:p.Met157=
NM_000644.2:c.470_471delinsTG	NP_000635.2:p.Met157=
NM_000645.2:c.419_420delinsTG	NP_000636.2:p.Met140=
NM_000646.2:c.422_423delinsTG	NP_000637.2:p.Met141=
XM_005270557.1:c.470_471delinsTG	XP_005270614.1:p.Met157=
XM_005270557.2:c.470_471delinsTG	XP_005270614.1:p.Met157=
NM_000642.3:c.470_471delinsTG MANE Select	NP_000633.2:p.Met157=