Canonical Allele Identifier: CA2038370021
Gene: MIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450323C= , CM000674.2:g.56450323C= GRCh38
NC_000012.11:g.56844107C= , CM000674.1:g.56844107C= GRCh37
NC_000012.10:g.55130374C= NCBI36
NG_021397.1:g.9329G=
NG_021397.2:g.23844G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1373G= ENSP00000497190.1:n.*1373G=
ENST00000652304.1:c.*957G= MANE Select ENSP00000498622.1:n.*957G=
ENST00000257979.4:c.*957G= ENSP00000257979.4:n.*957G=
NM_012064.3:c.*957G= NP_036196.1:n.*957G=
XM_011538354.1:c.*957G= XP_011536656.1:n.*957G=
NM_012064.4:c.*957G= MANE Select NP_036196.1:n.*957G=
XM_017019306.1:c.*957G= XP_016874795.1:n.*957G=