Canonical Allele Identifier: CA2038369908
Gene: MIP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450175G= , CM000674.2:g.56450175G= GRCh38
NC_000012.11:g.56843959G= , CM000674.1:g.56843959G= GRCh37
NC_000012.10:g.55130226G= NCBI36
NG_021397.1:g.9477C=
NG_021397.2:g.23992C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1521C= ENSP00000497190.1:n.*1521C=
ENST00000652304.1:c.*1105C= MANE Select ENSP00000498622.1:n.*1105C=
ENST00000257979.4:c.*1105C= ENSP00000257979.4:n.*1105C=
NM_012064.3:c.*1105C= NP_036196.1:n.*1105C=
XM_011538354.1:c.*1105C= XP_011536656.1:n.*1105C=
NM_012064.4:c.*1105C= MANE Select NP_036196.1:n.*1105C=
XM_017019306.1:c.*1105C= XP_016874795.1:n.*1105C=
Search 100 bp 5'
Search 100 bp 3'