Canonical Allele Identifier: CA4288869

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73593934G>A , CM000669.2:g.73593934G>A	GRCh38
NC_000007.13:g.73008264G>A , CM000669.1:g.73008264G>A	GRCh37
NC_000007.12:g.72646200G>A	NCBI36
NG_009307.1:g.35607C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.2490C>T MANE Select	ENSP00000320886.3:p.Thr830=
ENST00000313375.7:c.2490C>T	ENSP00000320886.3:p.Thr830=
ENST00000345114.9:c.2339C>T	ENSP00000343767.5:n.2339C>T
ENST00000354613.5:c.2427C>T	ENSP00000346629.1:p.Thr809=
ENST00000414749.6:c.2484C>T	ENSP00000412330.2:p.Thr828=
ENST00000429400.6:c.2433C>T	ENSP00000406296.2:p.Thr811=
ENST00000434326.5:c.*332C>T	ENSP00000392636.1:n.*332C>T
NM_032951.2:c.2490C>T	NP_116569.1:p.Thr830=
NM_032952.2:c.2433C>T	NP_116570.1:p.Thr811=
NM_032953.2:c.2484C>T	NP_116571.1:p.Thr828=
NM_032954.2:c.2427C>T	NP_116572.1:p.Thr809=
XM_011516277.1:c.2685C>T	XP_011514579.1:p.Thr895=
XM_011516278.1:c.2682C>T	XP_011514580.1:p.Thr894=
XM_011516279.1:c.2631C>T	XP_011514581.1:p.Thr877=
XM_011516280.1:c.1989C>T	XP_011514582.1:p.Thr663=
XM_011516281.1:c.1662C>T	XP_011514583.1:p.Thr554=
XR_927475.1:n.2369C>T
NR_134541.1:n.2390C>T
XM_011516281.2:c.1662C>T	XP_011514583.1:p.Thr554=
XM_017012263.1:c.1581C>T	XP_016867752.1:p.Thr527=
XM_024446784.1:c.1659C>T	XP_024302552.1:p.Thr553=
XR_001744799.1:n.2564C>T
NM_032951.3:c.2490C>T MANE Select	NP_116569.1:p.Thr830=
NM_032952.3:c.2433C>T	NP_116570.1:p.Thr811=
NM_032953.3:c.2484C>T	NP_116571.1:p.Thr828=
NM_032954.3:c.2427C>T	NP_116572.1:p.Thr809=
NR_134541.2:n.2369C>T