Canonical Allele Identifier: CA741031247

Gene: AGL

Linked Data

• dbSNP Id: rs1488643166
• MyVariant Identifiers: chr1:g.100346021_100346023del (hg19) ; chr1:g.99880465_99880467del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99880468_99880470del , CM000663.2:g.99880468_99880470del	GRCh38
NC_000001.10:g.100346024_100346026del , CM000663.1:g.100346024_100346026del	GRCh37
NC_000001.9:g.100118612_100118614del	NCBI36
NG_012865.1:g.35385_35387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1736-164_1736-162del MANE Select	ENSP00000355106.3:n.1736-164_1736-162del
ENST00000637337.1:n.1947-164_1947-162del
ENST00000294724.8:c.1736-164_1736-162del	ENSP00000294724.4:n.1736-164_1736-162del
ENST00000361302.7:c.1688-164_1688-162del	ENSP00000354971.3:n.1688-164_1688-162del
ENST00000361522.4:c.1685-164_1685-162del	ENSP00000354635.4:n.1685-164_1685-162del
ENST00000361915.7:c.1736-164_1736-162del	ENSP00000355106.3:n.1736-164_1736-162del
ENST00000370161.6:c.1688-164_1688-162del	ENSP00000359180.2:n.1688-164_1688-162del
ENST00000370163.7:c.1736-164_1736-162del	ENSP00000359182.3:n.1736-164_1736-162del
ENST00000370165.7:c.1736-164_1736-162del	ENSP00000359184.3:n.1736-164_1736-162del
NM_000028.2:c.1736-164_1736-162del	NP_000019.2:n.1736-164_1736-162del
NM_000642.2:c.1736-164_1736-162del	NP_000633.2:n.1736-164_1736-162del
NM_000643.2:c.1736-164_1736-162del	NP_000634.2:n.1736-164_1736-162del
NM_000644.2:c.1736-164_1736-162del	NP_000635.2:n.1736-164_1736-162del
NM_000645.2:c.1685-164_1685-162del	NP_000636.2:n.1685-164_1685-162del
NM_000646.2:c.1688-164_1688-162del	NP_000637.2:n.1688-164_1688-162del
XM_005270557.1:c.1736-164_1736-162del	XP_005270614.1:n.1736-164_1736-162del
XM_005270557.2:c.1736-164_1736-162del	XP_005270614.1:n.1736-164_1736-162del
XM_017000501.2:c.-5-164_-5-162del	XP_016855990.1:n.-5-164_-5-162del
NM_000642.3:c.1736-164_1736-162del MANE Select	NP_000633.2:n.1736-164_1736-162del