Canonical Allele Identifier: CA797107
Gene: HIVEP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.41510904A>G , CM000663.2:g.41510904A>G GRCh38
NC_000001.10:g.41976575A>G , CM000663.1:g.41976575A>G GRCh37
NC_000001.9:g.41749162A>G NCBI36
NG_030026.1:g.530022T>C
NG_030026.2:g.530022T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372583.6:c.6768T>C MANE Select ENSP00000361664.1:p.Pro2256=
ENST00000643665.1:c.6765T>C ENSP00000494598.1:p.Pro2255=
ENST00000247584.6:c.6768T>C ENSP00000247584.5:p.Pro2256=
ENST00000372583.5:c.6768T>C ENSP00000361664.1:p.Pro2256=
ENST00000372584.5:c.6765T>C ENSP00000361665.1:p.Pro2255=
ENST00000460604.1:n.1695T>C
NM_001127714.2:c.6765T>C NP_001121186.1:p.Pro2255=
NM_024503.4:c.6768T>C NP_078779.2:p.Pro2256=
XM_006710808.2:c.6768T>C XP_006710871.1:p.Pro2256=
XM_011541884.1:c.6768T>C XP_011540186.1:p.Pro2256=
XM_011541884.2:c.6768T>C XP_011540186.1:p.Pro2256=
XM_017001992.1:c.6768T>C XP_016857481.1:p.Pro2256=
XM_017001993.2:c.6768T>C XP_016857482.1:p.Pro2256=
XM_017001994.2:c.6765T>C XP_016857483.1:p.Pro2255=
XM_024448789.1:c.6768T>C XP_024304557.1:p.Pro2256=
NM_024503.5:c.6768T>C MANE Select NP_078779.2:p.Pro2256=
NM_001127714.3:c.6765T>C NP_001121186.1:p.Pro2255=