Canonical Allele Identifier: CA2796111432

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450343A>T , CM000674.2:g.56450343A>T	GRCh38
NC_000012.11:g.56844127A>T , CM000674.1:g.56844127A>T	GRCh37
NC_000012.10:g.55130394A>T	NCBI36
NG_021397.1:g.9309T>A
NG_021397.2:g.23824T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1353T>A	ENSP00000497190.1:n.*1353T>A
ENST00000652304.1:c.*937T>A MANE Select	ENSP00000498622.1:n.*937T>A
ENST00000257979.4:c.*937T>A	ENSP00000257979.4:n.*937T>A
NM_012064.3:c.*937T>A	NP_036196.1:n.*937T>A
XM_011538354.1:c.*937T>A	XP_011536656.1:n.*937T>A
NM_012064.4:c.*937T>A MANE Select	NP_036196.1:n.*937T>A
XM_017019306.1:c.*937T>A	XP_016874795.1:n.*937T>A