Canonical Allele Identifier: CA1652669033
Gene: HACE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.104784421T= , CM000668.2:g.104784421T= GRCh38
NC_000006.11:g.105232296T= , CM000668.1:g.105232296T= GRCh37
NC_000006.10:g.105338989T= NCBI36
NG_046782.1:g.80499A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262903.9:c.1474A= MANE Select ENSP00000262903.4:p.Asn492=
ENST00000262903.8:c.1474A= ENSP00000262903.4:p.Asn492=
ENST00000369125.6:c.1474A= ENSP00000358121.2:p.Asn492=
ENST00000369127.8:n.2495A=
ENST00000416605.6:c.*1031A= ENSP00000392425.2:n.*1031A=
ENST00000517424.1:c.279A=
NM_020771.3:c.1474A= NP_065822.2:p.Asn492=
NR_104424.1:n.1845A=
XM_006715528.2:c.1372A= XP_006715591.1:p.Asn458=
XM_006715529.2:c.1342A= XP_006715592.1:p.Asn448=
XM_006715530.2:c.970A= XP_006715593.1:p.Asn324=
XM_011535989.1:c.988A= XP_011534291.1:p.Asn330=
XM_011535990.1:c.970A= XP_011534292.1:p.Asn324=
XM_011535991.1:c.892A= XP_011534293.1:p.Asn298=
XM_011535992.1:c.1474A= XP_011534294.1:p.Asn492=
XR_942529.1:n.1751A=
XR_942531.1:n.1751A=
NM_001321080.1:c.1342A= NP_001308009.1:p.Asn448=
NM_001321083.1:c.1372A= NP_001308012.1:p.Asn458=
NM_001321084.1:c.970A= NP_001308013.1:p.Asn324=
NM_001350554.1:c.1240A= NP_001337483.1:p.Asn414=
NM_001350555.1:c.1183A= NP_001337484.1:p.Asn395=
NM_001350556.1:c.988A= NP_001337485.1:p.Asn330=
NM_001350557.1:c.970A= NP_001337486.1:p.Asn324=
NM_001350558.1:c.970A= NP_001337487.1:p.Asn324=
NM_001350559.1:c.892A= NP_001337488.1:p.Asn298=
NM_001350560.1:c.691A= NP_001337489.1:p.Asn231=
NR_146787.1:n.1592A=
NR_146788.1:n.1762A=
NR_146789.1:n.1751A=
NR_146790.1:n.1751A=
NR_146791.1:n.1751A=
NR_146792.1:n.1845A=
XM_017011114.2:c.1240A= XP_016866603.1:p.Asn414=
XM_017011119.2:c.970A= XP_016866608.1:p.Asn324=
XM_017011122.1:c.892A= XP_016866611.1:p.Asn298=
XR_001743536.1:n.1751A=
XR_001743538.1:n.1751A=
XR_942529.2:n.1751A=
NM_020771.4:c.1474A= MANE Select NP_065822.2:p.Asn492=
NM_001321080.2:c.1342A= NP_001308009.1:p.Asn448=
NM_001321083.2:c.1372A= NP_001308012.1:p.Asn458=
NM_001321084.2:c.970A= NP_001308013.1:p.Asn324=
NM_001350554.2:c.1240A= NP_001337483.1:p.Asn414=
NM_001350555.2:c.1183A= NP_001337484.1:p.Asn395=
NM_001350556.2:c.988A= NP_001337485.1:p.Asn330=
NM_001350557.2:c.970A= NP_001337486.1:p.Asn324=
NM_001350558.2:c.970A= NP_001337487.1:p.Asn324=
NM_001350559.2:c.892A= NP_001337488.1:p.Asn298=
NM_001350560.2:c.691A= NP_001337489.1:p.Asn231=
NR_104424.2:n.1845A=
NR_146787.2:n.1592A=
NR_146788.2:n.1762A=
NR_146789.2:n.1751A=
NR_146790.2:n.1751A=
NR_146791.2:n.1751A=
NR_146792.2:n.1845A=