Canonical Allele Identifier: CA2038370017

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450317C= , CM000674.2:g.56450317C=	GRCh38
NC_000012.11:g.56844101C= , CM000674.1:g.56844101C=	GRCh37
NC_000012.10:g.55130368C=	NCBI36
NG_021397.1:g.9335G=
NG_021397.2:g.23850G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1379G=	ENSP00000497190.1:n.*1379G=
ENST00000652304.1:c.*963G= MANE Select	ENSP00000498622.1:n.*963G=
ENST00000257979.4:c.*963G=	ENSP00000257979.4:n.*963G=
NM_012064.3:c.*963G=	NP_036196.1:n.*963G=
XM_011538354.1:c.*963G=	XP_011536656.1:n.*963G=
NM_012064.4:c.*963G= MANE Select	NP_036196.1:n.*963G=
XM_017019306.1:c.*963G=	XP_016874795.1:n.*963G=