Canonical Allele Identifier: CA10386258

Gene: MID1IP1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38805491G>A , CM000685.2:g.38805491G>A	GRCh38
NC_000023.10:g.38664744G>A , CM000685.1:g.38664744G>A	GRCh37
NC_000023.9:g.38549688G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021242.6:c.545G>A MANE Select	NP_067065.1:p.Gly182Asp
ENST00000614558.3:c.545G>A MANE Select	ENSP00000483547.1:p.Gly182Asp
NM_001098790.1:c.545G>A	NP_001092260.1:p.Gly182Asp
NM_001098790.2:c.545G>A	NP_001092260.1:p.Gly182Asp
NM_001098791.1:c.545G>A	NP_001092261.1:p.Gly182Asp
NM_001098791.2:c.545G>A	NP_001092261.1:p.Gly182Asp
NM_021242.5:c.545G>A	NP_067065.1:p.Gly182Asp
ENST00000336949.6:c.545G>A	ENSP00000338706.6:p.Gly182Asp
ENST00000336949.7:c.545G>A	ENSP00000338706.6:p.Gly182Asp
ENST00000378474.3:c.545G>A	ENSP00000367735.3:p.Gly182Asp
ENST00000457894.4:c.545G>A	ENSP00000416670.1:p.Gly182Asp
ENST00000457894.5:c.545G>A	ENSP00000416670.1:p.Gly182Asp
ENST00000614558.2:c.545G>A	ENSP00000483547.1:p.Gly182Asp