Canonical Allele Identifier: CA741018936

Gene: AGL

Linked Data

• dbSNP Id: rs1465965566
• MyVariant Identifiers: chr1:g.100327725_100327726del (hg19) ; chr1:g.99862169_99862170del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99862169_99862170del , CM000663.2:g.99862169_99862170del	GRCh38
NC_000001.10:g.100327725_100327726del , CM000663.1:g.100327725_100327726del	GRCh37
NC_000001.9:g.100100313_100100314del	NCBI36
NG_012865.1:g.17086_17087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.294-88_294-87del MANE Select	ENSP00000355106.3:n.294-88_294-87del
ENST00000637337.1:n.505-88_505-87del
ENST00000294724.8:c.294-88_294-87del	ENSP00000294724.4:n.294-88_294-87del
ENST00000361302.7:c.246-88_246-87del	ENSP00000354971.3:n.246-88_246-87del
ENST00000361522.4:c.243-88_243-87del	ENSP00000354635.4:n.243-88_243-87del
ENST00000361915.7:c.294-88_294-87del	ENSP00000355106.3:n.294-88_294-87del
ENST00000370161.6:c.246-88_246-87del	ENSP00000359180.2:n.246-88_246-87del
ENST00000370163.7:c.294-88_294-87del	ENSP00000359182.3:n.294-88_294-87del
ENST00000370165.7:c.294-88_294-87del	ENSP00000359184.3:n.294-88_294-87del
NM_000028.2:c.294-88_294-87del	NP_000019.2:n.294-88_294-87del
NM_000642.2:c.294-88_294-87del	NP_000633.2:n.294-88_294-87del
NM_000643.2:c.294-88_294-87del	NP_000634.2:n.294-88_294-87del
NM_000644.2:c.294-88_294-87del	NP_000635.2:n.294-88_294-87del
NM_000645.2:c.243-88_243-87del	NP_000636.2:n.243-88_243-87del
NM_000646.2:c.246-88_246-87del	NP_000637.2:n.246-88_246-87del
XM_005270557.1:c.294-88_294-87del	XP_005270614.1:n.294-88_294-87del
XM_005270557.2:c.294-88_294-87del	XP_005270614.1:n.294-88_294-87del
NM_000642.3:c.294-88_294-87del MANE Select	NP_000633.2:n.294-88_294-87del