Canonical Allele Identifier: CA690194252
Gene: MIP HGNC NCBI

Linked Data

dbSNP Id: rs1433606506

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450189_56450192del , CM000674.2:g.56450189_56450192del GRCh38
NC_000012.11:g.56843973_56843976del , CM000674.1:g.56843973_56843976del GRCh37
NC_000012.10:g.55130240_55130243del NCBI36
NG_021397.1:g.9461_9464del
NG_021397.2:g.23976_23979del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1505_*1508del ENSP00000497190.1:n.*1505_*1508del
ENST00000652304.1:c.*1089_*1092del MANE Select ENSP00000498622.1:n.*1089_*1092del
ENST00000257979.4:c.*1089_*1092del ENSP00000257979.4:n.*1089_*1092del
NM_012064.3:c.*1089_*1092del NP_036196.1:n.*1089_*1092del
XM_011538354.1:c.*1089_*1092del XP_011536656.1:n.*1089_*1092del
NM_012064.4:c.*1089_*1092del MANE Select NP_036196.1:n.*1089_*1092del
XM_017019306.1:c.*1089_*1092del XP_016874795.1:n.*1089_*1092del