Canonical Allele Identifier: CA2038370013

Gene: MIP

Linked Data

• dbSNP Id: rs1868550324

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450315del , CM000674.2:g.56450315del	GRCh38
NC_000012.11:g.56844099del , CM000674.1:g.56844099del	GRCh37
NC_000012.10:g.55130366del	NCBI36
NG_021397.1:g.9337del
NG_021397.2:g.23852del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1381del	ENSP00000497190.1:n.*1381del
ENST00000652304.1:c.*965del MANE Select	ENSP00000498622.1:n.*965del
ENST00000257979.4:c.*965del	ENSP00000257979.4:n.*965del
NM_012064.3:c.*965del	NP_036196.1:n.*965del
XM_011538354.1:c.*965del	XP_011536656.1:n.*965del
NM_012064.4:c.*965del MANE Select	NP_036196.1:n.*965del
XM_017019306.1:c.*965del	XP_016874795.1:n.*965del