Canonical Allele Identifier: CA1285674

Gene: RGL1

Genomic Alleles

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

Transcript Alleles

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