Canonical Allele Identifier: CA2038369789

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450051_56450053delinsAAG , CM000674.2:g.56450051_56450053delinsAAG	GRCh38
NC_000012.11:g.56843835_56843837delinsAAG , CM000674.1:g.56843835_56843837delinsAAG	GRCh37
NC_000012.10:g.55130102_55130104delinsAAG	NCBI36
NG_021397.1:g.9599_9601delinsCTT
NG_021397.2:g.24114_24116delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1643_*1645delinsCTT	ENSP00000497190.1:n.*1643_*1645delinsCTT
ENST00000652304.1:c.*1227_*1229delinsCTT MANE Select	ENSP00000498622.1:n.*1227_*1229delinsCTT
ENST00000257979.4:c.*1227_*1229delinsCTT	ENSP00000257979.4:n.*1227_*1229delinsCTT
NM_012064.3:c.*1227_*1229delinsCTT	NP_036196.1:n.*1227_*1229delinsCTT
XM_011538354.1:c.*1227_*1229delinsCTT	XP_011536656.1:n.*1227_*1229delinsCTT
NM_012064.4:c.*1227_*1229delinsCTT MANE Select	NP_036196.1:n.*1227_*1229delinsCTT
XM_017019306.1:c.*1227_*1229delinsCTT	XP_016874795.1:n.*1227_*1229delinsCTT