Canonical Allele Identifier: CA3637280
Gene: HIVEP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12121673C>T , CM000668.2:g.12121673C>T GRCh38
NC_000006.11:g.12121906C>T , CM000668.1:g.12121906C>T GRCh37
NC_000006.10:g.12229892C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379388.7:c.1878C>T MANE Select ENSP00000368698.2:p.Gly626=
ENST00000379388.6:c.1878C>T ENSP00000368698.2:p.Gly626=
ENST00000442081.6:c.166+1739C>T ENSP00000409078.2:n.166+1739C>T
ENST00000541134.5:c.1878C>T ENSP00000445617.2:p.Gly626=
ENST00000627968.2:c.-4426C>T ENSP00000486543.1:n.-4426C>T
NM_002114.3:c.1878C>T NP_002105.3:p.Gly626=
XM_011514545.1:c.1950C>T XP_011512847.1:p.Gly650=
XM_011514546.1:c.1905C>T XP_011512848.1:p.Gly635=
XM_011514547.1:c.1905C>T XP_011512849.1:p.Gly635=
XM_011514548.1:c.1905C>T XP_011512850.1:p.Gly635=
XM_011514549.1:c.1905C>T XP_011512851.1:p.Gly635=
XM_011514550.1:c.1905C>T XP_011512852.1:p.Gly635=
XM_011514551.1:c.1878C>T XP_011512853.1:p.Gly626=
XM_011514552.1:c.1878C>T XP_011512854.1:p.Gly626=
XM_011514553.1:c.1878C>T XP_011512855.1:p.Gly626=
XM_011514554.1:c.1824C>T XP_011512856.1:p.Gly608=
XM_011514555.1:c.1845C>T XP_011512857.1:p.Gly615=
XM_011514546.2:c.1905C>T XP_011512848.1:p.Gly635=
XM_011514547.2:c.1905C>T XP_011512849.1:p.Gly635=
XM_011514548.2:c.1905C>T XP_011512850.1:p.Gly635=
XM_011514549.3:c.1905C>T XP_011512851.1:p.Gly635=
XM_011514550.2:c.1905C>T XP_011512852.1:p.Gly635=
XM_011514551.2:c.1878C>T XP_011512853.1:p.Gly626=
XM_011514552.2:c.1878C>T XP_011512854.1:p.Gly626=
XM_011514555.3:c.1845C>T XP_011512857.1:p.Gly615=
XM_017010800.1:c.1905C>T XP_016866289.1:p.Gly635=
XM_017010801.1:c.1905C>T XP_016866290.1:p.Gly635=
XM_017010802.1:c.1905C>T XP_016866291.1:p.Gly635=
XM_017010803.1:c.1905C>T XP_016866292.1:p.Gly635=
XM_017010804.1:c.1905C>T XP_016866293.1:p.Gly635=
XR_001743372.1:n.3103C>T
NM_002114.4:c.1878C>T MANE Select NP_002105.3:p.Gly626=