Canonical Allele Identifier: CA2796111431

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450326G>T , CM000674.2:g.56450326G>T	GRCh38
NC_000012.11:g.56844110G>T , CM000674.1:g.56844110G>T	GRCh37
NC_000012.10:g.55130377G>T	NCBI36
NG_021397.1:g.9326C>A
NG_021397.2:g.23841C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1370C>A	ENSP00000497190.1:n.*1370C>A
ENST00000652304.1:c.*954C>A MANE Select	ENSP00000498622.1:n.*954C>A
ENST00000257979.4:c.*954C>A	ENSP00000257979.4:n.*954C>A
NM_012064.3:c.*954C>A	NP_036196.1:n.*954C>A
XM_011538354.1:c.*954C>A	XP_011536656.1:n.*954C>A
NM_012064.4:c.*954C>A MANE Select	NP_036196.1:n.*954C>A
XM_017019306.1:c.*954C>A	XP_016874795.1:n.*954C>A