Canonical Allele Identifier: CA798488
Gene: HIVEP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.41584693G>T , CM000663.2:g.41584693G>T GRCh38
NC_000001.10:g.42050364G>T , CM000663.1:g.42050364G>T GRCh37
NC_000001.9:g.41822951G>T NCBI36
NG_030026.1:g.456233C>A
NG_030026.2:g.456233C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372583.6:c.105C>A MANE Select ENSP00000361664.1:p.Val35=
ENST00000643665.1:c.105C>A ENSP00000494598.1:p.Val35=
ENST00000247584.6:c.105C>A ENSP00000247584.5:p.Val35=
ENST00000372583.5:c.105C>A ENSP00000361664.1:p.Val35=
ENST00000372584.5:c.105C>A ENSP00000361665.1:p.Val35=
NM_001127714.2:c.105C>A NP_001121186.1:p.Val35=
NM_024503.4:c.105C>A NP_078779.2:p.Val35=
XM_006710808.2:c.105C>A XP_006710871.1:p.Val35=
XM_006710809.2:c.105C>A XP_006710872.1:p.Val35=
XM_011541884.1:c.105C>A XP_011540186.1:p.Val35=
XM_011541885.1:c.105C>A XP_011540187.1:p.Val35=
XM_011541886.1:c.105C>A XP_011540188.1:p.Val35=
XM_011541887.1:c.105C>A XP_011540189.1:p.Val35=
XR_426625.2:n.701C>A
XM_011541884.2:c.105C>A XP_011540186.1:p.Val35=
XM_011541885.3:c.105C>A XP_011540187.1:p.Val35=
XM_011541886.3:c.105C>A XP_011540188.1:p.Val35=
XM_011541887.3:c.105C>A XP_011540189.1:p.Val35=
XM_017001992.1:c.105C>A XP_016857481.1:p.Val35=
XM_017001993.2:c.105C>A XP_016857482.1:p.Val35=
XM_017001994.2:c.105C>A XP_016857483.1:p.Val35=
XM_024448789.1:c.105C>A XP_024304557.1:p.Val35=
XR_001737357.2:n.1597C>A
NM_024503.5:c.105C>A MANE Select NP_078779.2:p.Val35=
NM_001127714.3:c.105C>A NP_001121186.1:p.Val35=