Canonical Allele Identifier: CA2038369923

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450187_56450191delinsTACAC , CM000674.2:g.56450187_56450191delinsTACAC	GRCh38
NC_000012.11:g.56843971_56843975delinsTACAC , CM000674.1:g.56843971_56843975delinsTACAC	GRCh37
NC_000012.10:g.55130238_55130242delinsTACAC	NCBI36
NG_021397.1:g.9461_9465delinsGTGTA
NG_021397.2:g.23976_23980delinsGTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1505_*1509delinsGTGTA	ENSP00000497190.1:n.*1505_*1509delinsGTGTA
ENST00000652304.1:c.*1089_*1093delinsGTGTA MANE Select	ENSP00000498622.1:n.*1089_*1093delinsGTGTA
ENST00000257979.4:c.*1089_*1093delinsGTGTA	ENSP00000257979.4:n.*1089_*1093delinsGTGTA
NM_012064.3:c.*1089_*1093delinsGTGTA	NP_036196.1:n.*1089_*1093delinsGTGTA
XM_011538354.1:c.*1089_*1093delinsGTGTA	XP_011536656.1:n.*1089_*1093delinsGTGTA
NM_012064.4:c.*1089_*1093delinsGTGTA MANE Select	NP_036196.1:n.*1089_*1093delinsGTGTA
XM_017019306.1:c.*1089_*1093delinsGTGTA	XP_016874795.1:n.*1089_*1093delinsGTGTA