Canonical Allele Identifier: CA2038369863
Gene: MIP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450107A= , CM000674.2:g.56450107A= GRCh38
NC_000012.11:g.56843891A= , CM000674.1:g.56843891A= GRCh37
NC_000012.10:g.55130158A= NCBI36
NG_021397.1:g.9545T=
NG_021397.2:g.24060T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1589T= ENSP00000497190.1:n.*1589T=
ENST00000652304.1:c.*1173T= MANE Select ENSP00000498622.1:n.*1173T=
ENST00000257979.4:c.*1173T= ENSP00000257979.4:n.*1173T=
NM_012064.3:c.*1173T= NP_036196.1:n.*1173T=
XM_011538354.1:c.*1173T= XP_011536656.1:n.*1173T=
NM_012064.4:c.*1173T= MANE Select NP_036196.1:n.*1173T=
XM_017019306.1:c.*1173T= XP_016874795.1:n.*1173T=
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