Canonical Allele Identifier: CA2038369678

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56449940_56449964delinsAAGATCGCTTGAGCCCAGGATTTCT , CM000674.2:g.56449940_56449964delinsAAGATCGCTTGAGCCCAGGATTTCT	GRCh38
NC_000012.11:g.56843724_56843748delinsAAGATCGCTTGAGCCCAGGATTTCT , CM000674.1:g.56843724_56843748delinsAAGATCGCTTGAGCCCAGGATTTCT	GRCh37
NC_000012.10:g.55129991_55130015delinsAAGATCGCTTGAGCCCAGGATTTCT	NCBI36
NG_021397.1:g.9688_9712delinsAGAAATCCTGGGCTCAAGCGATCTT
NG_021397.2:g.24203_24227delinsAGAAATCCTGGGCTCAAGCGATCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1732_*1756delinsAGAAATCCTGGGCTCAAGCGATCTT	ENSP00000497190.1:n.*1732_*1756delinsAGAAATCCTGGGCTCAAGCGATCT...
ENST00000652304.1:c.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT MANE Select	ENSP00000498622.1:n.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCT...
ENST00000257979.4:c.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT	ENSP00000257979.4:n.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCT...
NM_012064.3:c.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT	NP_036196.1:n.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT
XM_011538354.1:c.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT	XP_011536656.1:n.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT
NM_012064.4:c.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT MANE Select	NP_036196.1:n.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT
XM_017019306.1:c.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT	XP_016874795.1:n.*1316_*1340delinsAGAAATCCTGGGCTCAAGCGATCTT