Canonical Allele Identifier: CA2038369792

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450052_56450053delinsAG , CM000674.2:g.56450052_56450053delinsAG	GRCh38
NC_000012.11:g.56843836_56843837delinsAG , CM000674.1:g.56843836_56843837delinsAG	GRCh37
NC_000012.10:g.55130103_55130104delinsAG	NCBI36
NG_021397.1:g.9599_9600delinsCT
NG_021397.2:g.24114_24115delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1643_*1644delinsCT	ENSP00000497190.1:n.*1643_*1644delinsCT
ENST00000652304.1:c.*1227_*1228delinsCT MANE Select	ENSP00000498622.1:n.*1227_*1228delinsCT
ENST00000257979.4:c.*1227_*1228delinsCT	ENSP00000257979.4:n.*1227_*1228delinsCT
NM_012064.3:c.*1227_*1228delinsCT	NP_036196.1:n.*1227_*1228delinsCT
XM_011538354.1:c.*1227_*1228delinsCT	XP_011536656.1:n.*1227_*1228delinsCT
NM_012064.4:c.*1227_*1228delinsCT MANE Select	NP_036196.1:n.*1227_*1228delinsCT
XM_017019306.1:c.*1227_*1228delinsCT	XP_016874795.1:n.*1227_*1228delinsCT