Canonical Allele Identifier: CA2038370000

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450310_56450322delinsCCCCCTACTACCA , CM000674.2:g.56450310_56450322delinsCCCCCTACTACCA	GRCh38
NC_000012.11:g.56844094_56844106delinsCCCCCTACTACCA , CM000674.1:g.56844094_56844106delinsCCCCCTACTACCA	GRCh37
NC_000012.10:g.55130361_55130373delinsCCCCCTACTACCA	NCBI36
NG_021397.1:g.9330_9342delinsTGGTAGTAGGGGG
NG_021397.2:g.23845_23857delinsTGGTAGTAGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1374_*1386delinsTGGTAGTAGGGGG	ENSP00000497190.1:n.*1374_*1386delinsTGGTAGTAGGGGG
ENST00000652304.1:c.*958_*970delinsTGGTAGTAGGGGG MANE Select	ENSP00000498622.1:n.*958_*970delinsTGGTAGTAGGGGG
ENST00000257979.4:c.*958_*970delinsTGGTAGTAGGGGG	ENSP00000257979.4:n.*958_*970delinsTGGTAGTAGGGGG
NM_012064.3:c.*958_*970delinsTGGTAGTAGGGGG	NP_036196.1:n.*958_*970delinsTGGTAGTAGGGGG
XM_011538354.1:c.*958_*970delinsTGGTAGTAGGGGG	XP_011536656.1:n.*958_*970delinsTGGTAGTAGGGGG
NM_012064.4:c.*958_*970delinsTGGTAGTAGGGGG MANE Select	NP_036196.1:n.*958_*970delinsTGGTAGTAGGGGG
XM_017019306.1:c.*958_*970delinsTGGTAGTAGGGGG	XP_016874795.1:n.*958_*970delinsTGGTAGTAGGGGG