Canonical Allele Identifier: CA2038369752

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450041_56450045delinsCAAAA , CM000674.2:g.56450041_56450045delinsCAAAA	GRCh38
NC_000012.11:g.56843825_56843829delinsCAAAA , CM000674.1:g.56843825_56843829delinsCAAAA	GRCh37
NC_000012.10:g.55130092_55130096delinsCAAAA	NCBI36
NG_021397.1:g.9607_9611delinsTTTTG
NG_021397.2:g.24122_24126delinsTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1651_*1655delinsTTTTG	ENSP00000497190.1:n.*1651_*1655delinsTTTTG
ENST00000652304.1:c.*1235_*1239delinsTTTTG MANE Select	ENSP00000498622.1:n.*1235_*1239delinsTTTTG
ENST00000257979.4:c.*1235_*1239delinsTTTTG	ENSP00000257979.4:n.*1235_*1239delinsTTTTG
NM_012064.3:c.*1235_*1239delinsTTTTG	NP_036196.1:n.*1235_*1239delinsTTTTG
XM_011538354.1:c.*1235_*1239delinsTTTTG	XP_011536656.1:n.*1235_*1239delinsTTTTG
NM_012064.4:c.*1235_*1239delinsTTTTG MANE Select	NP_036196.1:n.*1235_*1239delinsTTTTG
XM_017019306.1:c.*1235_*1239delinsTTTTG	XP_016874795.1:n.*1235_*1239delinsTTTTG