Canonical Allele Identifier: CA2577789241
Gene: ITIH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52799127_52799128del , CM000665.2:g.52799127_52799128del GRCh38
NC_000003.11:g.52833143_52833144del , CM000665.1:g.52833143_52833144del GRCh37
NC_000003.10:g.52808183_52808184del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000703834.1:c.789+36_789+37del ENSP00000515492.1:n.789+36_789+37del
ENST00000449956.3:c.789+36_789+37del MANE Select ENSP00000415769.2:n.789+36_789+37del
ENST00000416872.6:c.789+36_789+37del ENSP00000413922.2:n.789+36_789+37del
ENST00000449956.2:c.789+36_789+37del ENSP00000415769.2:n.789+36_789+37del
ENST00000463893.1:n.288+36_288+37del
ENST00000465243.6:n.313+36_313+37del
ENST00000621946.4:c.789+36_789+37del ENSP00000479928.1:n.789+36_789+37del
NM_002217.3:c.789+36_789+37del NP_002208.3:n.789+36_789+37del
XM_005265105.3:c.789+36_789+37del XP_005265162.1:n.789+36_789+37del
XM_006713129.2:c.789+36_789+37del XP_006713192.1:n.789+36_789+37del
XM_006713130.2:c.789+36_789+37del XP_006713193.1:n.789+36_789+37del
XM_005265105.5:c.789+36_789+37del XP_005265162.1:n.789+36_789+37del
XM_024453512.1:c.-94+36_-94+37del XP_024309280.1:n.-94+36_-94+37del
NM_001392019.1:c.789+36_789+37del NP_001378948.1:n.789+36_789+37del
NM_001392020.1:c.789+36_789+37del NP_001378949.1:n.789+36_789+37del
NM_001392021.1:c.789+36_789+37del NP_001378950.1:n.789+36_789+37del
NM_001392022.1:c.789+36_789+37del NP_001378951.1:n.789+36_789+37del
NM_001392023.1:c.768+36_768+37del NP_001378952.1:n.768+36_768+37del
NM_001392024.1:c.789+36_789+37del NP_001378953.1:n.789+36_789+37del
NM_001392025.1:c.789+36_789+37del NP_001378954.1:n.789+36_789+37del
NM_001392026.1:c.789+36_789+37del NP_001378955.1:n.789+36_789+37del
NM_001392027.1:c.789+36_789+37del NP_001378956.1:n.789+36_789+37del
NM_002217.4:c.789+36_789+37del MANE Select NP_002208.3:n.789+36_789+37del