Canonical Allele Identifier: CA2038369780

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450050_56450053delinsAAAG , CM000674.2:g.56450050_56450053delinsAAAG	GRCh38
NC_000012.11:g.56843834_56843837delinsAAAG , CM000674.1:g.56843834_56843837delinsAAAG	GRCh37
NC_000012.10:g.55130101_55130104delinsAAAG	NCBI36
NG_021397.1:g.9599_9602delinsCTTT
NG_021397.2:g.24114_24117delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1643_*1646delinsCTTT	ENSP00000497190.1:n.*1643_*1646delinsCTTT
ENST00000652304.1:c.*1227_*1230delinsCTTT MANE Select	ENSP00000498622.1:n.*1227_*1230delinsCTTT
ENST00000257979.4:c.*1227_*1230delinsCTTT	ENSP00000257979.4:n.*1227_*1230delinsCTTT
NM_012064.3:c.*1227_*1230delinsCTTT	NP_036196.1:n.*1227_*1230delinsCTTT
XM_011538354.1:c.*1227_*1230delinsCTTT	XP_011536656.1:n.*1227_*1230delinsCTTT
NM_012064.4:c.*1227_*1230delinsCTTT MANE Select	NP_036196.1:n.*1227_*1230delinsCTTT
XM_017019306.1:c.*1227_*1230delinsCTTT	XP_016874795.1:n.*1227_*1230delinsCTTT