Canonical Allele Identifier: CA1183946919

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99916566_99916567delinsGT , CM000663.2:g.99916566_99916567delinsGT	GRCh38
NC_000001.10:g.100382122_100382123delinsGT , CM000663.1:g.100382122_100382123delinsGT	GRCh37
NC_000001.9:g.100154710_100154711delinsGT	NCBI36
NG_012865.1:g.71483_71484delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4348-32_4348-31delinsGT MANE Select	ENSP00000355106.3:n.4348-32_4348-31delinsGT
ENST00000637337.1:n.4559-32_4559-31delinsGT
ENST00000294724.8:c.4348-32_4348-31delinsGT	ENSP00000294724.4:n.4348-32_4348-31delinsGT
ENST00000361302.7:c.4300-32_4300-31delinsGT	ENSP00000354971.3:n.4300-32_4300-31delinsGT
ENST00000361522.4:c.4297-32_4297-31delinsGT	ENSP00000354635.4:n.4297-32_4297-31delinsGT
ENST00000361915.7:c.4348-32_4348-31delinsGT	ENSP00000355106.3:n.4348-32_4348-31delinsGT
ENST00000370161.6:c.4300-32_4300-31delinsGT	ENSP00000359180.2:n.4300-32_4300-31delinsGT
ENST00000370163.7:c.4348-32_4348-31delinsGT	ENSP00000359182.3:n.4348-32_4348-31delinsGT
ENST00000370165.7:c.4348-32_4348-31delinsGT	ENSP00000359184.3:n.4348-32_4348-31delinsGT
NM_000028.2:c.4348-32_4348-31delinsGT	NP_000019.2:n.4348-32_4348-31delinsGT
NM_000642.2:c.4348-32_4348-31delinsGT	NP_000633.2:n.4348-32_4348-31delinsGT
NM_000643.2:c.4348-32_4348-31delinsGT	NP_000634.2:n.4348-32_4348-31delinsGT
NM_000644.2:c.4348-32_4348-31delinsGT	NP_000635.2:n.4348-32_4348-31delinsGT
NM_000645.2:c.4297-32_4297-31delinsGT	NP_000636.2:n.4297-32_4297-31delinsGT
NM_000646.2:c.4300-32_4300-31delinsGT	NP_000637.2:n.4300-32_4300-31delinsGT
XM_005270557.1:c.4348-32_4348-31delinsGT	XP_005270614.1:n.4348-32_4348-31delinsGT
XR_947626.1:n.1318-3350_1318-3349delinsAC
XR_947627.1:n.1207-3350_1207-3349delinsAC
XR_947628.1:n.1312-3350_1312-3349delinsAC
XR_947630.1:n.1250-3350_1250-3349delinsAC
XR_947632.1:n.1136-3350_1136-3349delinsAC
XR_947633.1:n.1247-3350_1247-3349delinsAC
XR_947634.1:n.661-3350_661-3349delinsAC
XR_947635.1:n.729-3350_729-3349delinsAC
XM_005270557.2:c.4348-32_4348-31delinsGT	XP_005270614.1:n.4348-32_4348-31delinsGT
XM_017000501.2:c.2608-32_2608-31delinsGT	XP_016855990.1:n.2608-32_2608-31delinsGT
NM_000642.3:c.4348-32_4348-31delinsGT MANE Select	NP_000633.2:n.4348-32_4348-31delinsGT