Canonical Allele Identifier: CA2563872586
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99851027T>G , CM000663.2:g.99851027T>G GRCh38
NC_000001.10:g.100316583T>G , CM000663.1:g.100316583T>G GRCh37
NC_000001.9:g.100089171T>G NCBI36
NG_012865.1:g.5944T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.-16T>G MANE Select ENSP00000355106.3:n.-16T>G
ENST00000294724.8:c.-16T>G ENSP00000294724.4:n.-16T>G
ENST00000361302.7:c.-207T>G ENSP00000354971.3:n.-207T>G
ENST00000361915.7:c.-16T>G ENSP00000355106.3:n.-16T>G
ENST00000370163.7:c.-16T>G ENSP00000359182.3:n.-16T>G
ENST00000370165.7:c.-8-8T>G ENSP00000359184.3:n.-8-8T>G
NM_000028.2:c.-16T>G NP_000019.2:n.-16T>G
NM_000642.2:c.-16T>G NP_000633.2:n.-16T>G
NM_000643.2:c.-16T>G NP_000634.2:n.-16T>G
NM_000644.2:c.-8-8T>G NP_000635.2:n.-8-8T>G
NM_000646.2:c.-207T>G NP_000637.2:n.-207T>G
XM_005270557.1:c.-16T>G XP_005270614.1:n.-16T>G
XM_005270557.2:c.-16T>G XP_005270614.1:n.-16T>G
NM_000642.3:c.-16T>G MANE Select NP_000633.2:n.-16T>G