Canonical Allele Identifier: CA1183941638
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99910733_99910736delinsTTGA , CM000663.2:g.99910733_99910736delinsTTGA GRCh38
NC_000001.10:g.100376289_100376292delinsTTGA , CM000663.1:g.100376289_100376292delinsTTGA GRCh37
NC_000001.9:g.100148877_100148880delinsTTGA NCBI36
NG_012865.1:g.65650_65653delinsTTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.3722_3725delinsTTGA MANE Select ENSP00000355106.3:p.Val1241=
ENST00000637337.1:n.3933_3936delinsTTGA
ENST00000294724.8:c.3722_3725delinsTTGA ENSP00000294724.4:p.Val1241=
ENST00000361302.7:c.3674_3677delinsTTGA ENSP00000354971.3:p.Val1225=
ENST00000361522.4:c.3671_3674delinsTTGA ENSP00000354635.4:p.Val1224=
ENST00000361915.7:c.3722_3725delinsTTGA ENSP00000355106.3:p.Val1241=
ENST00000370161.6:c.3674_3677delinsTTGA ENSP00000359180.2:p.Val1225=
ENST00000370163.7:c.3722_3725delinsTTGA ENSP00000359182.3:p.Val1241=
ENST00000370165.7:c.3722_3725delinsTTGA ENSP00000359184.3:p.Val1241=
NM_000028.2:c.3722_3725delinsTTGA NP_000019.2:p.Val1241=
NM_000642.2:c.3722_3725delinsTTGA NP_000633.2:p.Val1241=
NM_000643.2:c.3722_3725delinsTTGA NP_000634.2:p.Val1241=
NM_000644.2:c.3722_3725delinsTTGA NP_000635.2:p.Val1241=
NM_000645.2:c.3671_3674delinsTTGA NP_000636.2:p.Val1224=
NM_000646.2:c.3674_3677delinsTTGA NP_000637.2:p.Val1225=
XM_005270557.1:c.3722_3725delinsTTGA XP_005270614.1:p.Val1241=
XM_005270557.2:c.3722_3725delinsTTGA XP_005270614.1:p.Val1241=
XM_017000501.2:c.1982_1985delinsTTGA XP_016855990.1:p.Val661=
NM_000642.3:c.3722_3725delinsTTGA MANE Select NP_000633.2:p.Val1241=