Canonical Allele Identifier: CA1365036529
Gene: ITIH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52819221C= , CM000665.2:g.52819221C= GRCh38
NC_000003.11:g.52853237C= , CM000665.1:g.52853237C= GRCh37
NC_000003.10:g.52828277C= NCBI36
NG_016006.1:g.16481G=
NG_016006.2:g.16481G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266041.9:c.2077+172G= MANE Select ENSP00000266041.4:n.2077+172G=
ENST00000266041.8:c.2077+172G= ENSP00000266041.4:n.2077+172G=
ENST00000406595.5:c.1987+172G= ENSP00000384425.1:n.1987+172G=
ENST00000441637.2:c.1559+172G=
ENST00000461966.5:n.206+172G=
ENST00000468472.1:c.*2763G= ENSP00000422253.1:n.*2763G=
ENST00000481977.5:n.274+172G=
ENST00000485816.5:c.2092+172G= ENSP00000417824.1:n.2092+172G=
ENST00000491663.5:n.2269+172G=
ENST00000537897.5:n.2109+172G=
NM_001166449.1:c.1987+172G= NP_001159921.1:n.1987+172G=
NM_002218.4:c.2077+172G= NP_002209.2:n.2077+172G=
NM_002218.5:c.2077+172G= MANE Select NP_002209.2:n.2077+172G=
NM_001166449.2:c.1987+172G= NP_001159921.1:n.1987+172G=