Canonical Allele Identifier: CA2038369882
Gene: MIP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450129G= , CM000674.2:g.56450129G= GRCh38
NC_000012.11:g.56843913G= , CM000674.1:g.56843913G= GRCh37
NC_000012.10:g.55130180G= NCBI36
NG_021397.1:g.9523C=
NG_021397.2:g.24038C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1567C= ENSP00000497190.1:n.*1567C=
ENST00000652304.1:c.*1151C= MANE Select ENSP00000498622.1:n.*1151C=
ENST00000257979.4:c.*1151C= ENSP00000257979.4:n.*1151C=
NM_012064.3:c.*1151C= NP_036196.1:n.*1151C=
XM_011538354.1:c.*1151C= XP_011536656.1:n.*1151C=
NM_012064.4:c.*1151C= MANE Select NP_036196.1:n.*1151C=
XM_017019306.1:c.*1151C= XP_016874795.1:n.*1151C=
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