Canonical Allele Identifier: CA655095616
Gene: MIP HGNC NCBI

Linked Data

COSMIC: COSN21434148
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450312_56450313insT , CM000674.2:g.56450312_56450313insT GRCh38
NC_000012.11:g.56844096_56844097insT , CM000674.1:g.56844096_56844097insT GRCh37
NC_000012.10:g.55130363_55130364insT NCBI36
NG_021397.1:g.9339_9340insA
NG_021397.2:g.23854_23855insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1383_*1384insA ENSP00000497190.1:n.*1383_*1384insA
ENST00000652304.1:c.*967_*968insA MANE Select ENSP00000498622.1:n.*967_*968insA
ENST00000257979.4:c.*967_*968insA ENSP00000257979.4:n.*967_*968insA
NM_012064.3:c.*967_*968insA NP_036196.1:n.*967_*968insA
XM_011538354.1:c.*967_*968insA XP_011536656.1:n.*967_*968insA
NM_012064.4:c.*967_*968insA MANE Select NP_036196.1:n.*967_*968insA
XM_017019306.1:c.*967_*968insA XP_016874795.1:n.*967_*968insA
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