Canonical Allele Identifier: CA1183929228

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99881185_99881186delinsTA , CM000663.2:g.99881185_99881186delinsTA	GRCh38
NC_000001.10:g.100346741_100346742delinsTA , CM000663.1:g.100346741_100346742delinsTA	GRCh37
NC_000001.9:g.100119329_100119330delinsTA	NCBI36
NG_012865.1:g.36102_36103delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.2001+8_2001+9delinsTA MANE Select	ENSP00000355106.3:n.2001+8_2001+9delinsTA
ENST00000637337.1:n.2212+8_2212+9delinsTA
ENST00000294724.8:c.2001+8_2001+9delinsTA	ENSP00000294724.4:n.2001+8_2001+9delinsTA
ENST00000361302.7:c.1953+8_1953+9delinsTA	ENSP00000354971.3:n.1953+8_1953+9delinsTA
ENST00000361522.4:c.1950+8_1950+9delinsTA	ENSP00000354635.4:n.1950+8_1950+9delinsTA
ENST00000361915.7:c.2001+8_2001+9delinsTA	ENSP00000355106.3:n.2001+8_2001+9delinsTA
ENST00000370161.6:c.1953+8_1953+9delinsTA	ENSP00000359180.2:n.1953+8_1953+9delinsTA
ENST00000370163.7:c.2001+8_2001+9delinsTA	ENSP00000359182.3:n.2001+8_2001+9delinsTA
ENST00000370165.7:c.2001+8_2001+9delinsTA	ENSP00000359184.3:n.2001+8_2001+9delinsTA
NM_000028.2:c.2001+8_2001+9delinsTA	NP_000019.2:n.2001+8_2001+9delinsTA
NM_000642.2:c.2001+8_2001+9delinsTA	NP_000633.2:n.2001+8_2001+9delinsTA
NM_000643.2:c.2001+8_2001+9delinsTA	NP_000634.2:n.2001+8_2001+9delinsTA
NM_000644.2:c.2001+8_2001+9delinsTA	NP_000635.2:n.2001+8_2001+9delinsTA
NM_000645.2:c.1950+8_1950+9delinsTA	NP_000636.2:n.1950+8_1950+9delinsTA
NM_000646.2:c.1953+8_1953+9delinsTA	NP_000637.2:n.1953+8_1953+9delinsTA
XM_005270557.1:c.2001+8_2001+9delinsTA	XP_005270614.1:n.2001+8_2001+9delinsTA
XM_005270557.2:c.2001+8_2001+9delinsTA	XP_005270614.1:n.2001+8_2001+9delinsTA
XM_017000501.2:c.261+8_261+9delinsTA	XP_016855990.1:n.261+8_261+9delinsTA
NM_000642.3:c.2001+8_2001+9delinsTA MANE Select	NP_000633.2:n.2001+8_2001+9delinsTA