Canonical Allele Identifier: CA2744753099
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99851020T>C , CM000663.2:g.99851020T>C GRCh38
NC_000001.10:g.100316576T>C , CM000663.1:g.100316576T>C GRCh37
NC_000001.9:g.100089164T>C NCBI36
NG_012865.1:g.5937T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.-23T>C MANE Select ENSP00000355106.3:n.-23T>C
ENST00000294724.8:c.-23T>C ENSP00000294724.4:n.-23T>C
ENST00000361302.7:c.-214T>C ENSP00000354971.3:n.-214T>C
ENST00000361915.7:c.-23T>C ENSP00000355106.3:n.-23T>C
ENST00000370163.7:c.-23T>C ENSP00000359182.3:n.-23T>C
ENST00000370165.7:c.-8-15T>C ENSP00000359184.3:n.-8-15T>C
NM_000028.2:c.-23T>C NP_000019.2:n.-23T>C
NM_000642.2:c.-23T>C NP_000633.2:n.-23T>C
NM_000643.2:c.-23T>C NP_000634.2:n.-23T>C
NM_000644.2:c.-8-15T>C NP_000635.2:n.-8-15T>C
NM_000646.2:c.-214T>C NP_000637.2:n.-214T>C
XM_005270557.1:c.-23T>C XP_005270614.1:n.-23T>C
XM_005270557.2:c.-23T>C XP_005270614.1:n.-23T>C
NM_000642.3:c.-23T>C MANE Select NP_000633.2:n.-23T>C