Canonical Allele Identifier: CA4288860

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73593903G>A , CM000669.2:g.73593903G>A	GRCh38
NC_000007.13:g.73008233G>A , CM000669.1:g.73008233G>A	GRCh37
NC_000007.12:g.72646169G>A	NCBI36
NG_009307.1:g.35638C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.2521C>T MANE Select	ENSP00000320886.3:p.Arg841Trp
ENST00000313375.7:c.2521C>T	ENSP00000320886.3:p.Arg841Trp
ENST00000345114.9:c.2370C>T	ENSP00000343767.5:n.2370C>T
ENST00000354613.5:c.2458C>T	ENSP00000346629.1:p.Arg820Trp
ENST00000414749.6:c.2515C>T	ENSP00000412330.2:p.Arg839Trp
ENST00000429400.6:c.2464C>T	ENSP00000406296.2:p.Arg822Trp
ENST00000434326.5:c.*363C>T	ENSP00000392636.1:n.*363C>T
NM_032951.2:c.2521C>T	NP_116569.1:p.Arg841Trp
NM_032952.2:c.2464C>T	NP_116570.1:p.Arg822Trp
NM_032953.2:c.2515C>T	NP_116571.1:p.Arg839Trp
NM_032954.2:c.2458C>T	NP_116572.1:p.Arg820Trp
XM_011516277.1:c.2716C>T	XP_011514579.1:p.Arg906Trp
XM_011516278.1:c.2713C>T	XP_011514580.1:p.Arg905Trp
XM_011516279.1:c.2662C>T	XP_011514581.1:p.Arg888Trp
XM_011516280.1:c.2020C>T	XP_011514582.1:p.Arg674Trp
XM_011516281.1:c.1693C>T	XP_011514583.1:p.Arg565Trp
XR_927475.1:n.2400C>T
NR_134541.1:n.2421C>T
XM_011516281.2:c.1693C>T	XP_011514583.1:p.Arg565Trp
XM_017012263.1:c.1612C>T	XP_016867752.1:p.Arg538Trp
XM_024446784.1:c.1690C>T	XP_024302552.1:p.Arg564Trp
XR_001744799.1:n.2595C>T
NM_032951.3:c.2521C>T MANE Select	NP_116569.1:p.Arg841Trp
NM_032952.3:c.2464C>T	NP_116570.1:p.Arg822Trp
NM_032953.3:c.2515C>T	NP_116571.1:p.Arg839Trp
NM_032954.3:c.2458C>T	NP_116572.1:p.Arg820Trp
NR_134541.2:n.2400C>T