Canonical Allele Identifier: CA4289267

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73597579G>C , CM000669.2:g.73597579G>C	GRCh38
NC_000007.13:g.73011909G>C , CM000669.1:g.73011909G>C	GRCh37
NC_000007.12:g.72649845G>C	NCBI36
NG_009307.1:g.31962C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.1206C>G MANE Select	ENSP00000320886.3:p.Ala402=
ENST00000313375.7:c.1206C>G	ENSP00000320886.3:p.Ala402=
ENST00000345114.9:c.1206C>G	ENSP00000343767.5:p.Ala402=
ENST00000354613.5:c.1206C>G	ENSP00000346629.1:p.Ala402=
ENST00000414749.6:c.1206C>G	ENSP00000412330.2:p.Ala402=
ENST00000429400.6:c.1206C>G	ENSP00000406296.2:p.Ala402=
ENST00000434326.5:c.927C>G	ENSP00000392636.1:p.Ala309=
ENST00000476404.5:n.1301C>G
NM_032951.2:c.1206C>G	NP_116569.1:p.Ala402=
NM_032952.2:c.1206C>G	NP_116570.1:p.Ala402=
NM_032953.2:c.1206C>G	NP_116571.1:p.Ala402=
NM_032954.2:c.1206C>G	NP_116572.1:p.Ala402=
XM_011516277.1:c.1401C>G	XP_011514579.1:p.Ala467=
XM_011516278.1:c.1401C>G	XP_011514580.1:p.Ala467=
XM_011516279.1:c.1401C>G	XP_011514581.1:p.Ala467=
XM_011516280.1:c.705C>G	XP_011514582.1:p.Ala235=
XM_011516281.1:c.378C>G	XP_011514583.1:p.Ala126=
XR_927474.1:n.1431C>G
XR_927475.1:n.1236C>G
NR_134541.1:n.1257C>G
XM_011516281.2:c.378C>G	XP_011514583.1:p.Ala126=
XM_017012263.1:c.297C>G	XP_016867752.1:p.Ala99=
XM_024446784.1:c.378C>G	XP_024302552.1:p.Ala126=
XR_001744799.1:n.1431C>G
NM_032951.3:c.1206C>G MANE Select	NP_116569.1:p.Ala402=
NM_032952.3:c.1206C>G	NP_116570.1:p.Ala402=
NM_032953.3:c.1206C>G	NP_116571.1:p.Ala402=
NM_032954.3:c.1206C>G	NP_116572.1:p.Ala402=
NR_134541.2:n.1236C>G