Canonical Allele Identifier: CA741018998

Gene: AGL

Linked Data

• dbSNP Id: rs1460439618
• MyVariant Identifiers: chr1:g.100376233_100376237del (hg19) ; chr1:g.99910677_99910681del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99910679_99910683del , CM000663.2:g.99910679_99910683del	GRCh38
NC_000001.10:g.100376235_100376239del , CM000663.1:g.100376235_100376239del	GRCh37
NC_000001.9:g.100148823_100148827del	NCBI36
NG_012865.1:g.65596_65600del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3701-33_3701-29del MANE Select	ENSP00000355106.3:n.3701-33_3701-29del
ENST00000637337.1:n.3912-33_3912-29del
ENST00000294724.8:c.3701-33_3701-29del	ENSP00000294724.4:n.3701-33_3701-29del
ENST00000361302.7:c.3653-33_3653-29del	ENSP00000354971.3:n.3653-33_3653-29del
ENST00000361522.4:c.3650-33_3650-29del	ENSP00000354635.4:n.3650-33_3650-29del
ENST00000361915.7:c.3701-33_3701-29del	ENSP00000355106.3:n.3701-33_3701-29del
ENST00000370161.6:c.3653-33_3653-29del	ENSP00000359180.2:n.3653-33_3653-29del
ENST00000370163.7:c.3701-33_3701-29del	ENSP00000359182.3:n.3701-33_3701-29del
ENST00000370165.7:c.3701-33_3701-29del	ENSP00000359184.3:n.3701-33_3701-29del
NM_000028.2:c.3701-33_3701-29del	NP_000019.2:n.3701-33_3701-29del
NM_000642.2:c.3701-33_3701-29del	NP_000633.2:n.3701-33_3701-29del
NM_000643.2:c.3701-33_3701-29del	NP_000634.2:n.3701-33_3701-29del
NM_000644.2:c.3701-33_3701-29del	NP_000635.2:n.3701-33_3701-29del
NM_000645.2:c.3650-33_3650-29del	NP_000636.2:n.3650-33_3650-29del
NM_000646.2:c.3653-33_3653-29del	NP_000637.2:n.3653-33_3653-29del
XM_005270557.1:c.3701-33_3701-29del	XP_005270614.1:n.3701-33_3701-29del
XM_005270557.2:c.3701-33_3701-29del	XP_005270614.1:n.3701-33_3701-29del
XM_017000501.2:c.1961-33_1961-29del	XP_016855990.1:n.1961-33_1961-29del
NM_000642.3:c.3701-33_3701-29del MANE Select	NP_000633.2:n.3701-33_3701-29del