Canonical Allele Identifier: CA1212083731
Gene: RGL1 HGNC NCBI

Linked Data

dbSNP Id: rs10797919

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183883780G>T , CM000663.2:g.183883780G>T GRCh38
NC_000001.10:g.183852914G>T , CM000663.1:g.183852914G>T GRCh37
NC_000001.9:g.182119537G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360851.4:c.611-6G>T MANE Select ENSP00000354097.3:n.611-6G>T
ENST00000304685.8:c.716-6G>T ENSP00000303192.3:n.716-6G>T
ENST00000360851.3:c.611-6G>T ENSP00000354097.3:n.611-6G>T
NM_001297669.1:c.605-6G>T NP_001284598.1:n.605-6G>T
NM_001297670.1:c.605-6G>T NP_001284599.1:n.605-6G>T
NM_001297671.1:c.611-6G>T NP_001284600.1:n.611-6G>T
NM_001297672.1:c.611-6G>T NP_001284601.1:n.611-6G>T
NM_015149.4:c.716-6G>T NP_055964.3:n.716-6G>T
XM_011509339.1:c.716-6G>T XP_011507641.1:n.716-6G>T
XM_011509340.1:c.716-6G>T XP_011507642.1:n.716-6G>T
XM_011509341.1:c.716-6G>T XP_011507643.1:n.716-6G>T
XM_011509342.1:c.716-6G>T XP_011507644.1:n.716-6G>T
XM_011509339.3:c.716-6G>T XP_011507641.1:n.716-6G>T
XM_011509342.2:c.716-6G>T XP_011507644.1:n.716-6G>T
XM_017000756.2:c.611-6G>T XP_016856245.1:n.611-6G>T
NM_001297669.2:c.605-6G>T NP_001284598.1:n.605-6G>T
NM_001297670.2:c.605-6G>T NP_001284599.1:n.605-6G>T
NM_001297671.2:c.611-6G>T NP_001284600.1:n.611-6G>T
NM_001297672.2:c.611-6G>T NP_001284601.1:n.611-6G>T
NM_015149.5:c.716-6G>T NP_055964.3:n.716-6G>T
NM_001297669.3:c.605-6G>T NP_001284598.1:n.605-6G>T
NM_001297670.3:c.605-6G>T NP_001284599.1:n.605-6G>T
NM_001297671.3:c.611-6G>T MANE Select NP_001284600.1:n.611-6G>T
NM_001297672.3:c.611-6G>T NP_001284601.1:n.611-6G>T
NM_015149.6:c.716-6G>T NP_055964.3:n.716-6G>T