Canonical Allele Identifier: CA2038369700

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56449978_56449979delinsCG , CM000674.2:g.56449978_56449979delinsCG	GRCh38
NC_000012.11:g.56843762_56843763delinsCG , CM000674.1:g.56843762_56843763delinsCG	GRCh37
NC_000012.10:g.55130029_55130030delinsCG	NCBI36
NG_021397.1:g.9673_9674delinsCG
NG_021397.2:g.24188_24189delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1717_*1718delinsCG	ENSP00000497190.1:n.*1717_*1718delinsCG
ENST00000652304.1:c.*1301_*1302delinsCG MANE Select	ENSP00000498622.1:n.*1301_*1302delinsCG
ENST00000257979.4:c.*1301_*1302delinsCG	ENSP00000257979.4:n.*1301_*1302delinsCG
NM_012064.3:c.*1301_*1302delinsCG	NP_036196.1:n.*1301_*1302delinsCG
XM_011538354.1:c.*1301_*1302delinsCG	XP_011536656.1:n.*1301_*1302delinsCG
NM_012064.4:c.*1301_*1302delinsCG MANE Select	NP_036196.1:n.*1301_*1302delinsCG
XM_017019306.1:c.*1301_*1302delinsCG	XP_016874795.1:n.*1301_*1302delinsCG