Canonical Allele Identifier: CA2038369902

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450173_56450175delinsCAG , CM000674.2:g.56450173_56450175delinsCAG	GRCh38
NC_000012.11:g.56843957_56843959delinsCAG , CM000674.1:g.56843957_56843959delinsCAG	GRCh37
NC_000012.10:g.55130224_55130226delinsCAG	NCBI36
NG_021397.1:g.9477_9479delinsCTG
NG_021397.2:g.23992_23994delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1521_*1523delinsCTG	ENSP00000497190.1:n.*1521_*1523delinsCTG
ENST00000652304.1:c.*1105_*1107delinsCTG MANE Select	ENSP00000498622.1:n.*1105_*1107delinsCTG
ENST00000257979.4:c.*1105_*1107delinsCTG	ENSP00000257979.4:n.*1105_*1107delinsCTG
NM_012064.3:c.*1105_*1107delinsCTG	NP_036196.1:n.*1105_*1107delinsCTG
XM_011538354.1:c.*1105_*1107delinsCTG	XP_011536656.1:n.*1105_*1107delinsCTG
NM_012064.4:c.*1105_*1107delinsCTG MANE Select	NP_036196.1:n.*1105_*1107delinsCTG
XM_017019306.1:c.*1105_*1107delinsCTG	XP_016874795.1:n.*1105_*1107delinsCTG