Canonical Allele Identifier: CA2619338739

Gene: MIP

Linked Data

• gnomAD v4: 12-56450320-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450320C>A , CM000674.2:g.56450320C>A	GRCh38
NC_000012.11:g.56844104C>A , CM000674.1:g.56844104C>A	GRCh37
NC_000012.10:g.55130371C>A	NCBI36
NG_021397.1:g.9332G>T
NG_021397.2:g.23847G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1376G>T	ENSP00000497190.1:n.*1376G>T
ENST00000652304.1:c.*960G>T MANE Select	ENSP00000498622.1:n.*960G>T
ENST00000257979.4:c.*960G>T	ENSP00000257979.4:n.*960G>T
NM_012064.3:c.*960G>T	NP_036196.1:n.*960G>T
XM_011538354.1:c.*960G>T	XP_011536656.1:n.*960G>T
NM_012064.4:c.*960G>T MANE Select	NP_036196.1:n.*960G>T
XM_017019306.1:c.*960G>T	XP_016874795.1:n.*960G>T