Canonical Allele Identifier: CA2038370029
Gene: MIP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450324C= , CM000674.2:g.56450324C= GRCh38
NC_000012.11:g.56844108C= , CM000674.1:g.56844108C= GRCh37
NC_000012.10:g.55130375C= NCBI36
NG_021397.1:g.9328G=
NG_021397.2:g.23843G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1372G= ENSP00000497190.1:n.*1372G=
ENST00000652304.1:c.*956G= MANE Select ENSP00000498622.1:n.*956G=
ENST00000257979.4:c.*956G= ENSP00000257979.4:n.*956G=
NM_012064.3:c.*956G= NP_036196.1:n.*956G=
XM_011538354.1:c.*956G= XP_011536656.1:n.*956G=
NM_012064.4:c.*956G= MANE Select NP_036196.1:n.*956G=
XM_017019306.1:c.*956G= XP_016874795.1:n.*956G=
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