Canonical Allele Identifier: CA2038370011

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450314_56450315delinsCT , CM000674.2:g.56450314_56450315delinsCT	GRCh38
NC_000012.11:g.56844098_56844099delinsCT , CM000674.1:g.56844098_56844099delinsCT	GRCh37
NC_000012.10:g.55130365_55130366delinsCT	NCBI36
NG_021397.1:g.9337_9338delinsAG
NG_021397.2:g.23852_23853delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1381_*1382delinsAG	ENSP00000497190.1:n.*1381_*1382delinsAG
ENST00000652304.1:c.*965_*966delinsAG MANE Select	ENSP00000498622.1:n.*965_*966delinsAG
ENST00000257979.4:c.*965_*966delinsAG	ENSP00000257979.4:n.*965_*966delinsAG
NM_012064.3:c.*965_*966delinsAG	NP_036196.1:n.*965_*966delinsAG
XM_011538354.1:c.*965_*966delinsAG	XP_011536656.1:n.*965_*966delinsAG
NM_012064.4:c.*965_*966delinsAG MANE Select	NP_036196.1:n.*965_*966delinsAG
XM_017019306.1:c.*965_*966delinsAG	XP_016874795.1:n.*965_*966delinsAG