Canonical Allele Identifier: CA2038369891

Gene: MIP

Linked Data

• dbSNP Id: rs1868542715

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450141_56450145del , CM000674.2:g.56450141_56450145del	GRCh38
NC_000012.11:g.56843925_56843929del , CM000674.1:g.56843925_56843929del	GRCh37
NC_000012.10:g.55130192_55130196del	NCBI36
NG_021397.1:g.9510_9514del
NG_021397.2:g.24025_24029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1554_*1558del	ENSP00000497190.1:n.*1554_*1558del
ENST00000652304.1:c.*1138_*1142del MANE Select	ENSP00000498622.1:n.*1138_*1142del
ENST00000257979.4:c.*1138_*1142del	ENSP00000257979.4:n.*1138_*1142del
NM_012064.3:c.*1138_*1142del	NP_036196.1:n.*1138_*1142del
XM_011538354.1:c.*1138_*1142del	XP_011536656.1:n.*1138_*1142del
NM_012064.4:c.*1138_*1142del MANE Select	NP_036196.1:n.*1138_*1142del
XM_017019306.1:c.*1138_*1142del	XP_016874795.1:n.*1138_*1142del