Canonical Allele Identifier: CA966417

Gene: AGL

Linked Data

• dbSNP Id: rs770463818
• ExAC: 1:100340852 T / TA
• gnomAD v2: 1-100340852-T-TA
• gnomAD v3: 1-99875296-T-TA
• gnomAD v4: 1-99875296-T-TA
• MyVariant Identifiers: chr1:g.100340852_100340853insA (hg19) ; chr1:g.99875296_99875297insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99875297dup , CM000663.2:g.99875297dup	GRCh38
NC_000001.10:g.100340853dup , CM000663.1:g.100340853dup	GRCh37
NC_000001.9:g.100113441dup	NCBI36
NG_012865.1:g.30214dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.1185+41dup MANE Select	ENSP00000355106.3:n.1185+41dup
ENST00000637337.1:n.1396+41dup
ENST00000294724.8:c.1185+41dup	ENSP00000294724.4:n.1185+41dup
ENST00000361302.7:c.1137+41dup	ENSP00000354971.3:n.1137+41dup
ENST00000361522.4:c.1134+41dup	ENSP00000354635.4:n.1134+41dup
ENST00000361915.7:c.1185+41dup	ENSP00000355106.3:n.1185+41dup
ENST00000370161.6:c.1137+41dup	ENSP00000359180.2:n.1137+41dup
ENST00000370163.7:c.1185+41dup	ENSP00000359182.3:n.1185+41dup
ENST00000370165.7:c.1185+41dup	ENSP00000359184.3:n.1185+41dup
ENST00000477753.1:n.444+41dup
NM_000028.2:c.1185+41dup	NP_000019.2:n.1185+41dup
NM_000642.2:c.1185+41dup	NP_000633.2:n.1185+41dup
NM_000643.2:c.1185+41dup	NP_000634.2:n.1185+41dup
NM_000644.2:c.1185+41dup	NP_000635.2:n.1185+41dup
NM_000645.2:c.1134+41dup	NP_000636.2:n.1134+41dup
NM_000646.2:c.1137+41dup	NP_000637.2:n.1137+41dup
XM_005270557.1:c.1185+41dup	XP_005270614.1:n.1185+41dup
XM_005270557.2:c.1185+41dup	XP_005270614.1:n.1185+41dup
NM_000642.3:c.1185+41dup MANE Select	NP_000633.2:n.1185+41dup