Canonical Allele Identifier: CA2038369989

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450298T= , CM000674.2:g.56450298T=	GRCh38
NC_000012.11:g.56844082T= , CM000674.1:g.56844082T=	GRCh37
NC_000012.10:g.55130349T=	NCBI36
NG_021397.1:g.9354A=
NG_021397.2:g.23869A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1398A=	ENSP00000497190.1:n.*1398A=
ENST00000652304.1:c.*982A= MANE Select	ENSP00000498622.1:n.*982A=
ENST00000257979.4:c.*982A=	ENSP00000257979.4:n.*982A=
NM_012064.3:c.*982A=	NP_036196.1:n.*982A=
XM_011538354.1:c.*982A=	XP_011536656.1:n.*982A=
NM_012064.4:c.*982A= MANE Select	NP_036196.1:n.*982A=
XM_017019306.1:c.*982A=	XP_016874795.1:n.*982A=