Canonical Allele Identifier: CA967377
Gene: AGL HGNC NCBI

Linked Data

dbSNP Id: rs757025800

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99916395dup , CM000663.2:g.99916395dup GRCh38
NC_000001.10:g.100381951dup , CM000663.1:g.100381951dup GRCh37
NC_000001.9:g.100154539dup NCBI36
NG_012865.1:g.71312dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.4260-15dup MANE Select ENSP00000355106.3:n.4260-15dup
ENST00000637337.1:n.4471-15dup
ENST00000294724.8:c.4260-15dup ENSP00000294724.4:n.4260-15dup
ENST00000361302.7:c.4212-15dup ENSP00000354971.3:n.4212-15dup
ENST00000361522.4:c.4209-15dup ENSP00000354635.4:n.4209-15dup
ENST00000361915.7:c.4260-15dup ENSP00000355106.3:n.4260-15dup
ENST00000370161.6:c.4212-15dup ENSP00000359180.2:n.4212-15dup
ENST00000370163.7:c.4260-15dup ENSP00000359182.3:n.4260-15dup
ENST00000370165.7:c.4260-15dup ENSP00000359184.3:n.4260-15dup
NM_000028.2:c.4260-15dup NP_000019.2:n.4260-15dup
NM_000642.2:c.4260-15dup NP_000633.2:n.4260-15dup
NM_000643.2:c.4260-15dup NP_000634.2:n.4260-15dup
NM_000644.2:c.4260-15dup NP_000635.2:n.4260-15dup
NM_000645.2:c.4209-15dup NP_000636.2:n.4209-15dup
NM_000646.2:c.4212-15dup NP_000637.2:n.4212-15dup
XM_005270557.1:c.4260-15dup XP_005270614.1:n.4260-15dup
XR_947626.1:n.1318-3176dup
XR_947627.1:n.1207-3176dup
XR_947628.1:n.1312-3176dup
XR_947630.1:n.1250-3176dup
XR_947632.1:n.1136-3176dup
XR_947633.1:n.1247-3176dup
XR_947634.1:n.661-3176dup
XR_947635.1:n.729-3176dup
XM_005270557.2:c.4260-15dup XP_005270614.1:n.4260-15dup
XM_017000501.2:c.2520-15dup XP_016855990.1:n.2520-15dup
NM_000642.3:c.4260-15dup MANE Select NP_000633.2:n.4260-15dup