Canonical Allele Identifier: CA2557758888

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56449990del , CM000674.2:g.56449990del	GRCh38
NC_000012.11:g.56843774del , CM000674.1:g.56843774del	GRCh37
NC_000012.10:g.55130041del	NCBI36
NG_021397.1:g.9663del
NG_021397.2:g.24178del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1707del	ENSP00000497190.1:n.*1707del
ENST00000652304.1:c.*1291del MANE Select	ENSP00000498622.1:n.*1291del
ENST00000257979.4:c.*1291del	ENSP00000257979.4:n.*1291del
NM_012064.3:c.*1291del	NP_036196.1:n.*1291del
XM_011538354.1:c.*1291del	XP_011536656.1:n.*1291del
NM_012064.4:c.*1291del MANE Select	NP_036196.1:n.*1291del
XM_017019306.1:c.*1291del	XP_016874795.1:n.*1291del