Canonical Allele Identifier: CA2038369996
Gene: MIP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450308T= , CM000674.2:g.56450308T= GRCh38
NC_000012.11:g.56844092T= , CM000674.1:g.56844092T= GRCh37
NC_000012.10:g.55130359T= NCBI36
NG_021397.1:g.9344A=
NG_021397.2:g.23859A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1388A= ENSP00000497190.1:n.*1388A=
ENST00000652304.1:c.*972A= MANE Select ENSP00000498622.1:n.*972A=
ENST00000257979.4:c.*972A= ENSP00000257979.4:n.*972A=
NM_012064.3:c.*972A= NP_036196.1:n.*972A=
XM_011538354.1:c.*972A= XP_011536656.1:n.*972A=
NM_012064.4:c.*972A= MANE Select NP_036196.1:n.*972A=
XM_017019306.1:c.*972A= XP_016874795.1:n.*972A=
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