Canonical Allele Identifier: CA2038369729

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450016_56450017delinsTG , CM000674.2:g.56450016_56450017delinsTG	GRCh38
NC_000012.11:g.56843800_56843801delinsTG , CM000674.1:g.56843800_56843801delinsTG	GRCh37
NC_000012.10:g.55130067_55130068delinsTG	NCBI36
NG_021397.1:g.9635_9636delinsCA
NG_021397.2:g.24150_24151delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1679_*1680delinsCA	ENSP00000497190.1:n.*1679_*1680delinsCA
ENST00000652304.1:c.*1263_*1264delinsCA MANE Select	ENSP00000498622.1:n.*1263_*1264delinsCA
ENST00000257979.4:c.*1263_*1264delinsCA	ENSP00000257979.4:n.*1263_*1264delinsCA
NM_012064.3:c.*1263_*1264delinsCA	NP_036196.1:n.*1263_*1264delinsCA
XM_011538354.1:c.*1263_*1264delinsCA	XP_011536656.1:n.*1263_*1264delinsCA
NM_012064.4:c.*1263_*1264delinsCA MANE Select	NP_036196.1:n.*1263_*1264delinsCA
XM_017019306.1:c.*1263_*1264delinsCA	XP_016874795.1:n.*1263_*1264delinsCA