Canonical Allele Identifier: CA2619338645

Gene: MIP

Linked Data

• gnomAD v4: 12-56450152-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450153del , CM000674.2:g.56450153del	GRCh38
NC_000012.11:g.56843937del , CM000674.1:g.56843937del	GRCh37
NC_000012.10:g.55130204del	NCBI36
NG_021397.1:g.9499del
NG_021397.2:g.24014del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1543del	ENSP00000497190.1:n.*1543del
ENST00000652304.1:c.*1127del MANE Select	ENSP00000498622.1:n.*1127del
ENST00000257979.4:c.*1127del	ENSP00000257979.4:n.*1127del
NM_012064.3:c.*1127del	NP_036196.1:n.*1127del
XM_011538354.1:c.*1127del	XP_011536656.1:n.*1127del
NM_012064.4:c.*1127del MANE Select	NP_036196.1:n.*1127del
XM_017019306.1:c.*1127del	XP_016874795.1:n.*1127del