Canonical Allele Identifier: CA1183926876

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99875465_99875469delinsTTTTG , CM000663.2:g.99875465_99875469delinsTTTTG	GRCh38
NC_000001.10:g.100341021_100341025delinsTTTTG , CM000663.1:g.100341021_100341025delinsTTTTG	GRCh37
NC_000001.9:g.100113609_100113613delinsTTTTG	NCBI36
NG_012865.1:g.30382_30386delinsTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1283+10_1283+14delinsTTTTG MANE Select	ENSP00000355106.3:n.1283+10_1283+14delinsTTTTG
ENST00000637337.1:n.1494+10_1494+14delinsTTTTG
ENST00000294724.8:c.1283+10_1283+14delinsTTTTG	ENSP00000294724.4:n.1283+10_1283+14delinsTTTTG
ENST00000361302.7:c.1235+10_1235+14delinsTTTTG	ENSP00000354971.3:n.1235+10_1235+14delinsTTTTG
ENST00000361522.4:c.1232+10_1232+14delinsTTTTG	ENSP00000354635.4:n.1232+10_1232+14delinsTTTTG
ENST00000361915.7:c.1283+10_1283+14delinsTTTTG	ENSP00000355106.3:n.1283+10_1283+14delinsTTTTG
ENST00000370161.6:c.1235+10_1235+14delinsTTTTG	ENSP00000359180.2:n.1235+10_1235+14delinsTTTTG
ENST00000370163.7:c.1283+10_1283+14delinsTTTTG	ENSP00000359182.3:n.1283+10_1283+14delinsTTTTG
ENST00000370165.7:c.1283+10_1283+14delinsTTTTG	ENSP00000359184.3:n.1283+10_1283+14delinsTTTTG
ENST00000477753.1:n.542+10_542+14delinsTTTTG
NM_000028.2:c.1283+10_1283+14delinsTTTTG	NP_000019.2:n.1283+10_1283+14delinsTTTTG
NM_000642.2:c.1283+10_1283+14delinsTTTTG	NP_000633.2:n.1283+10_1283+14delinsTTTTG
NM_000643.2:c.1283+10_1283+14delinsTTTTG	NP_000634.2:n.1283+10_1283+14delinsTTTTG
NM_000644.2:c.1283+10_1283+14delinsTTTTG	NP_000635.2:n.1283+10_1283+14delinsTTTTG
NM_000645.2:c.1232+10_1232+14delinsTTTTG	NP_000636.2:n.1232+10_1232+14delinsTTTTG
NM_000646.2:c.1235+10_1235+14delinsTTTTG	NP_000637.2:n.1235+10_1235+14delinsTTTTG
XM_005270557.1:c.1283+10_1283+14delinsTTTTG	XP_005270614.1:n.1283+10_1283+14delinsTTTTG
XM_005270557.2:c.1283+10_1283+14delinsTTTTG	XP_005270614.1:n.1283+10_1283+14delinsTTTTG
NM_000642.3:c.1283+10_1283+14delinsTTTTG MANE Select	NP_000633.2:n.1283+10_1283+14delinsTTTTG