Canonical Allele Identifier: CA6989784

Gene: ALG11

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.52012462G>C , CM000675.2:g.52012462G>C	GRCh38
NC_000013.10:g.52586598G>C , CM000675.1:g.52586598G>C	GRCh37
NC_000013.9:g.51484599G>C	NCBI36
NG_008806.1:g.4033C>G
NG_028038.1:g.5076G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521508.2:c.44G>C MANE Select	ENSP00000430236.1:p.Arg15Thr
ENST00000649340.2:c.44G>C	ENSP00000497184.2:p.Arg15Thr
ENST00000649708.2:c.44G>C	ENSP00000497459.2:p.Arg15Thr
ENST00000650049.2:c.44G>C	ENSP00000497398.2:p.Arg15Thr
ENST00000679359.1:c.44G>C	ENSP00000505579.1:p.Arg15Thr
ENST00000679495.1:n.44G>C
ENST00000679544.1:c.44G>C	ENSP00000505560.1:p.Arg15Thr
ENST00000680793.1:n.65G>C
ENST00000680950.1:n.59G>C
ENST00000681047.1:c.44G>C	ENSP00000505034.1:p.Arg15Thr
ENST00000681053.1:c.44G>C	ENSP00000505307.1:p.Arg15Thr
ENST00000681145.1:c.44G>C	ENSP00000505163.1:p.Arg15Thr
ENST00000681226.1:n.52G>C
ENST00000521508.1:c.44G>C	ENSP00000430236.1:p.Arg15Thr
ENST00000523764.1:c.44G>C	ENSP00000429497.1:p.Arg15Thr
ENST00000616513.1:c.44G>C	ENSP00000481922.1:p.Ser15Thr
NM_001004127.2:c.44G>C	NP_001004127.2:p.Arg15Thr
NR_036571.2:n.76G>C
NM_001004127.3:c.44G>C MANE Select	NP_001004127.2:p.Arg15Thr
NR_036571.3:n.65G>C