Canonical Allele Identifier: CA2038370005

Gene: MIP

Linked Data

• dbSNP Id: rs1868549812

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450314_56450325del , CM000674.2:g.56450314_56450325del	GRCh38
NC_000012.11:g.56844098_56844109del , CM000674.1:g.56844098_56844109del	GRCh37
NC_000012.10:g.55130365_55130376del	NCBI36
NG_021397.1:g.9330_9341del
NG_021397.2:g.23845_23856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1374_*1385del	ENSP00000497190.1:n.*1374_*1385del
ENST00000652304.1:c.*958_*969del MANE Select	ENSP00000498622.1:n.*958_*969del
ENST00000257979.4:c.*958_*969del	ENSP00000257979.4:n.*958_*969del
NM_012064.3:c.*958_*969del	NP_036196.1:n.*958_*969del
XM_011538354.1:c.*958_*969del	XP_011536656.1:n.*958_*969del
NM_012064.4:c.*958_*969del MANE Select	NP_036196.1:n.*958_*969del
XM_017019306.1:c.*958_*969del	XP_016874795.1:n.*958_*969del