Canonical Allele Identifier: CA2619338729

Gene: MIP

Linked Data

• gnomAD v4: 12-56450309-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450314dup , CM000674.2:g.56450314dup	GRCh38
NC_000012.11:g.56844098dup , CM000674.1:g.56844098dup	GRCh37
NC_000012.10:g.55130365dup	NCBI36
NG_021397.1:g.9342dup
NG_021397.2:g.23857dup

Transcript Alleles

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