Canonical Allele Identifier: CA12472476
Gene: MLXIPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73602675A>G , CM000669.2:g.73602675A>G GRCh38
NC_000007.13:g.73017005A>G , CM000669.1:g.73017005A>G GRCh37
NC_000007.12:g.72654941A>G NCBI36
NG_009307.1:g.26866T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313375.8:c.902-2980T>C MANE Select ENSP00000320886.3:n.902-2980T>C
ENST00000313375.7:c.902-2980T>C ENSP00000320886.3:n.902-2980T>C
ENST00000345114.9:c.902-2980T>C ENSP00000343767.5:n.902-2980T>C
ENST00000354613.5:c.902-2980T>C ENSP00000346629.1:n.902-2980T>C
ENST00000414749.6:c.902-2980T>C ENSP00000412330.2:n.902-2980T>C
ENST00000429400.6:c.902-2980T>C ENSP00000406296.2:n.902-2980T>C
ENST00000434326.5:c.623-2980T>C ENSP00000392636.1:n.623-2980T>C
ENST00000453275.1:c.401-2980T>C ENSP00000395172.1:n.401-2980T>C
ENST00000476404.5:n.997-2980T>C
ENST00000488212.1:n.431-2980T>C
NM_032951.2:c.902-2980T>C NP_116569.1:n.902-2980T>C
NM_032952.2:c.902-2980T>C NP_116570.1:n.902-2980T>C
NM_032953.2:c.902-2980T>C NP_116571.1:n.902-2980T>C
NM_032954.2:c.902-2980T>C NP_116572.1:n.902-2980T>C
XM_011516277.1:c.1097-2980T>C XP_011514579.1:n.1097-2980T>C
XM_011516278.1:c.1097-2980T>C XP_011514580.1:n.1097-2980T>C
XM_011516279.1:c.1097-2980T>C XP_011514581.1:n.1097-2980T>C
XM_011516280.1:c.401-2980T>C XP_011514582.1:n.401-2980T>C
XM_011516281.1:c.73+720T>C XP_011514583.1:n.73+720T>C
XR_927474.1:n.1127-2980T>C
XR_927475.1:n.932-2980T>C
NR_134541.1:n.953-2980T>C
XM_011516281.2:c.73+720T>C XP_011514583.1:n.73+720T>C
XM_017012263.1:c.22-3009T>C XP_016867752.1:n.22-3009T>C
XM_024446784.1:c.73+720T>C XP_024302552.1:n.73+720T>C
XR_001744799.1:n.1127-2980T>C
NM_032951.3:c.902-2980T>C MANE Select NP_116569.1:n.902-2980T>C
NM_032952.3:c.902-2980T>C NP_116570.1:n.902-2980T>C
NM_032953.3:c.902-2980T>C NP_116571.1:n.902-2980T>C
NM_032954.3:c.902-2980T>C NP_116572.1:n.902-2980T>C
NR_134541.2:n.932-2980T>C
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