Canonical Allele Identifier: CA213871851

Gene: MXI1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110246728G>T , CM000672.2:g.110246728G>T	GRCh38
NC_000010.10:g.112006486G>T , CM000672.1:g.112006486G>T	GRCh37
NC_000010.9:g.111996476G>T	NCBI36
NG_012103.1:g.44124G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650644.1:c.128+1871G>T	ENSP00000498900.1:n.128+1871G>T
ENST00000650696.1:c.128+1871G>T	ENSP00000499158.1:n.128+1871G>T
ENST00000650752.1:c.128+1871G>T	ENSP00000499134.1:n.128+1871G>T
ENST00000650810.1:c.128+1871G>T	ENSP00000498390.1:n.128+1871G>T
ENST00000650843.1:c.128+1871G>T	ENSP00000498547.1:n.128+1871G>T
ENST00000650900.1:c.128+1871G>T	ENSP00000499209.1:n.128+1871G>T
ENST00000650952.1:c.128+1871G>T	ENSP00000499161.1:n.128+1871G>T
ENST00000651004.1:c.128+1871G>T	ENSP00000498396.1:n.128+1871G>T
ENST00000651109.1:c.128+1871G>T	ENSP00000498214.1:n.128+1871G>T
ENST00000651112.1:c.29+1871G>T	ENSP00000498951.1:n.29+1871G>T
ENST00000651167.1:c.128+1871G>T	ENSP00000498764.1:n.128+1871G>T
ENST00000651225.1:c.*225+1871G>T	ENSP00000498220.1:n.*225+1871G>T
ENST00000651318.1:c.128+1871G>T	ENSP00000498911.1:n.128+1871G>T
ENST00000651467.1:c.128+1871G>T	ENSP00000499128.1:n.128+1871G>T
ENST00000651495.1:c.128+1871G>T	ENSP00000498536.1:n.128+1871G>T
ENST00000651516.1:c.128+1871G>T	ENSP00000498873.1:n.128+1871G>T
ENST00000651557.1:c.*12+1855G>T	ENSP00000498474.1:n.*12+1855G>T
ENST00000651613.1:c.128+1871G>T	ENSP00000498554.1:n.128+1871G>T
ENST00000651811.1:c.128+1871G>T	ENSP00000498472.1:n.128+1871G>T
ENST00000651848.1:c.128+1871G>T	ENSP00000498238.1:n.128+1871G>T
ENST00000651866.1:c.128+1871G>T	ENSP00000498306.1:n.128+1871G>T
ENST00000652028.1:c.128+1871G>T	ENSP00000498928.1:n.128+1871G>T
ENST00000652243.1:c.128+1871G>T	ENSP00000498409.1:n.128+1871G>T
ENST00000652323.1:c.204+910G>T	ENSP00000498637.1:n.204+910G>T
ENST00000652463.1:c.128+1871G>T	ENSP00000499087.1:n.128+1871G>T
ENST00000652506.1:c.128+1871G>T	ENSP00000498573.1:n.128+1871G>T
ENST00000652604.1:c.98+18407G>T	ENSP00000498971.1:n.98+18407G>T
ENST00000652649.1:c.*189+1871G>T	ENSP00000499130.1:n.*189+1871G>T
ENST00000239007.11:c.236+1871G>T	ENSP00000239007.7:n.236+1871G>T
ENST00000332674.9:c.437+1871G>T MANE Select	ENSP00000331152.5:n.437+1871G>T
ENST00000361248.8:c.98+18407G>T	ENSP00000354606.4:n.98+18407G>T
ENST00000369612.1:c.128+1871G>T	ENSP00000358625.1:n.128+1871G>T
ENST00000393134.5:c.206+18407G>T	ENSP00000376842.1:n.206+18407G>T
ENST00000442296.5:c.128+1871G>T	ENSP00000407711.1:n.128+1871G>T
ENST00000453116.5:c.407+18407G>T	ENSP00000398981.1:n.407+18407G>T
ENST00000460667.5:n.428+1855G>T
ENST00000484030.5:n.260+910G>T
ENST00000485566.1:n.785+910G>T
NM_001008541.1:c.98+18407G>T	NP_001008541.1:n.98+18407G>T
NM_005962.4:c.236+1871G>T	NP_005953.4:n.236+1871G>T
NM_130439.3:c.437+1871G>T MANE Select	NP_569157.2:n.437+1871G>T
NM_005962.5:c.236+1871G>T	NP_005953.4:n.236+1871G>T