Canonical Allele Identifier: CA1365020091
Gene: ITIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52783619A= , CM000665.2:g.52783619A= GRCh38
NC_000003.11:g.52817635A= , CM000665.1:g.52817635A= GRCh37
NC_000003.10:g.52792675A= NCBI36
NG_016005.1:g.11028A=

Transcript Alleles

HGVS Amino-acid change
ENST00000273283.7:c.1225+280A= MANE Select ENSP00000273283.2:n.1225+280A=
ENST00000273283.6:c.1225+280A= ENSP00000273283.2:n.1225+280A=
ENST00000537050.5:c.361+280A= ENSP00000443847.1:n.361+280A=
ENST00000628722.2:n.1080+280A=
NM_001166434.2:c.799+280A= NP_001159906.1:n.799+280A=
NM_001166435.2:c.361+280A= NP_001159907.1:n.361+280A=
NM_001166436.2:c.361+280A= NP_001159908.1:n.361+280A=
NM_002215.3:c.1225+280A= NP_002206.2:n.1225+280A=
NM_002215.4:c.1225+280A= MANE Select NP_002206.2:n.1225+280A=
NM_001166434.3:c.799+280A= NP_001159906.1:n.799+280A=