Canonical Allele Identifier: CA2619338750

Gene: MIP

Linked Data

• gnomAD v4: 12-56450338-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450338G>A , CM000674.2:g.56450338G>A	GRCh38
NC_000012.11:g.56844122G>A , CM000674.1:g.56844122G>A	GRCh37
NC_000012.10:g.55130389G>A	NCBI36
NG_021397.1:g.9314C>T
NG_021397.2:g.23829C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1358C>T	ENSP00000497190.1:n.*1358C>T
ENST00000652304.1:c.*942C>T MANE Select	ENSP00000498622.1:n.*942C>T
ENST00000257979.4:c.*942C>T	ENSP00000257979.4:n.*942C>T
NM_012064.3:c.*942C>T	NP_036196.1:n.*942C>T
XM_011538354.1:c.*942C>T	XP_011536656.1:n.*942C>T
NM_012064.4:c.*942C>T MANE Select	NP_036196.1:n.*942C>T
XM_017019306.1:c.*942C>T	XP_016874795.1:n.*942C>T