Canonical Allele Identifier: CA605264539
Gene: MIP HGNC NCBI

Linked Data

dbSNP Id: rs1265250693
gnomAD v2: 12-56843831-A-AT
gnomAD v3: 12-56450047-A-AT
gnomAD v4: 12-56450047-A-AT
MyVariant Identifiers: chr12:g.56843831_56843832insT (hg19) chr12:g.56450047_56450048insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450047_56450048insT , CM000674.2:g.56450047_56450048insT GRCh38
NC_000012.11:g.56843831_56843832insT , CM000674.1:g.56843831_56843832insT GRCh37
NC_000012.10:g.55130098_55130099insT NCBI36
NG_021397.1:g.9604_9605insA
NG_021397.2:g.24119_24120insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1648_*1649insA ENSP00000497190.1:n.*1648_*1649insA
ENST00000652304.1:c.*1232_*1233insA MANE Select ENSP00000498622.1:n.*1232_*1233insA
ENST00000257979.4:c.*1232_*1233insA ENSP00000257979.4:n.*1232_*1233insA
NM_012064.3:c.*1232_*1233insA NP_036196.1:n.*1232_*1233insA
XM_011538354.1:c.*1232_*1233insA XP_011536656.1:n.*1232_*1233insA
NM_012064.4:c.*1232_*1233insA MANE Select NP_036196.1:n.*1232_*1233insA
XM_017019306.1:c.*1232_*1233insA XP_016874795.1:n.*1232_*1233insA
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