Canonical Allele Identifier: CA34308409

Gene: RGL1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183867898A>G , CM000663.2:g.183867898A>G	GRCh38
NC_000001.10:g.183837032A>G , CM000663.1:g.183837032A>G	GRCh37
NC_000001.9:g.182103655A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360851.4:c.425+1825A>G MANE Select	ENSP00000354097.3:n.425+1825A>G
ENST00000304685.8:c.530+1825A>G	ENSP00000303192.3:n.530+1825A>G
ENST00000360851.3:c.425+1825A>G	ENSP00000354097.3:n.425+1825A>G
NM_001297669.1:c.419+1825A>G	NP_001284598.1:n.419+1825A>G
NM_001297670.1:c.419+1825A>G	NP_001284599.1:n.419+1825A>G
NM_001297671.1:c.425+1825A>G	NP_001284600.1:n.425+1825A>G
NM_001297672.1:c.425+1825A>G	NP_001284601.1:n.425+1825A>G
NM_015149.4:c.530+1825A>G	NP_055964.3:n.530+1825A>G
XM_011509339.1:c.530+1825A>G	XP_011507641.1:n.530+1825A>G
XM_011509340.1:c.530+1825A>G	XP_011507642.1:n.530+1825A>G
XM_011509341.1:c.530+1825A>G	XP_011507643.1:n.530+1825A>G
XM_011509342.1:c.530+1825A>G	XP_011507644.1:n.530+1825A>G
XM_011509339.3:c.530+1825A>G	XP_011507641.1:n.530+1825A>G
XM_011509342.2:c.530+1825A>G	XP_011507644.1:n.530+1825A>G
XM_017000756.2:c.425+1825A>G	XP_016856245.1:n.425+1825A>G
NM_001297669.2:c.419+1825A>G	NP_001284598.1:n.419+1825A>G
NM_001297670.2:c.419+1825A>G	NP_001284599.1:n.419+1825A>G
NM_001297671.2:c.425+1825A>G	NP_001284600.1:n.425+1825A>G
NM_001297672.2:c.425+1825A>G	NP_001284601.1:n.425+1825A>G
NM_015149.5:c.530+1825A>G	NP_055964.3:n.530+1825A>G
NM_001297669.3:c.419+1825A>G	NP_001284598.1:n.419+1825A>G
NM_001297670.3:c.419+1825A>G	NP_001284599.1:n.419+1825A>G
NM_001297671.3:c.425+1825A>G MANE Select	NP_001284600.1:n.425+1825A>G
NM_001297672.3:c.425+1825A>G	NP_001284601.1:n.425+1825A>G
NM_015149.6:c.530+1825A>G	NP_055964.3:n.530+1825A>G