Canonical Allele Identifier: CA2038369802

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450054A= , CM000674.2:g.56450054A=	GRCh38
NC_000012.11:g.56843838A= , CM000674.1:g.56843838A=	GRCh37
NC_000012.10:g.55130105A=	NCBI36
NG_021397.1:g.9598T=
NG_021397.2:g.24113T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1642T=	ENSP00000497190.1:n.*1642T=
ENST00000652304.1:c.*1226T= MANE Select	ENSP00000498622.1:n.*1226T=
ENST00000257979.4:c.*1226T=	ENSP00000257979.4:n.*1226T=
NM_012064.3:c.*1226T=	NP_036196.1:n.*1226T=
XM_011538354.1:c.*1226T=	XP_011536656.1:n.*1226T=
NM_012064.4:c.*1226T= MANE Select	NP_036196.1:n.*1226T=
XM_017019306.1:c.*1226T=	XP_016874795.1:n.*1226T=