Canonical Allele Identifier: CA365135959

Gene: HACE1

Linked Data

• MyVariant Identifiers: chr6:g.105232318A>T (hg19) ; chr6:g.104784443A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.104784443A>T , CM000668.2:g.104784443A>T	GRCh38
NC_000006.11:g.105232318A>T , CM000668.1:g.105232318A>T	GRCh37
NC_000006.10:g.105339011A>T	NCBI36
NG_046782.1:g.80477T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262903.9:c.1452T>A MANE Select	ENSP00000262903.4:p.Asp484Glu
ENST00000262903.8:c.1452T>A	ENSP00000262903.4:p.Asp484Glu
ENST00000369125.6:c.1452T>A	ENSP00000358121.2:p.Asp484Glu
ENST00000369127.8:n.2473T>A
ENST00000416605.6:c.*1009T>A	ENSP00000392425.2:n.*1009T>A
ENST00000517424.1:c.257T>A
NM_020771.3:c.1452T>A	NP_065822.2:p.Asp484Glu
NR_104424.1:n.1823T>A
XM_006715528.2:c.1350T>A	XP_006715591.1:p.Asp450Glu
XM_006715529.2:c.1320T>A	XP_006715592.1:p.Asp440Glu
XM_006715530.2:c.948T>A	XP_006715593.1:p.Asp316Glu
XM_011535989.1:c.966T>A	XP_011534291.1:p.Asp322Glu
XM_011535990.1:c.948T>A	XP_011534292.1:p.Asp316Glu
XM_011535991.1:c.870T>A	XP_011534293.1:p.Asp290Glu
XM_011535992.1:c.1452T>A	XP_011534294.1:p.Asp484Glu
XR_942529.1:n.1729T>A
XR_942531.1:n.1729T>A
NM_001321080.1:c.1320T>A	NP_001308009.1:p.Asp440Glu
NM_001321083.1:c.1350T>A	NP_001308012.1:p.Asp450Glu
NM_001321084.1:c.948T>A	NP_001308013.1:p.Asp316Glu
NM_001350554.1:c.1218T>A	NP_001337483.1:p.Asp406Glu
NM_001350555.1:c.1161T>A	NP_001337484.1:p.Asp387Glu
NM_001350556.1:c.966T>A	NP_001337485.1:p.Asp322Glu
NM_001350557.1:c.948T>A	NP_001337486.1:p.Asp316Glu
NM_001350558.1:c.948T>A	NP_001337487.1:p.Asp316Glu
NM_001350559.1:c.870T>A	NP_001337488.1:p.Asp290Glu
NM_001350560.1:c.669T>A	NP_001337489.1:p.Asp223Glu
NR_146787.1:n.1570T>A
NR_146788.1:n.1740T>A
NR_146789.1:n.1729T>A
NR_146790.1:n.1729T>A
NR_146791.1:n.1729T>A
NR_146792.1:n.1823T>A
XM_017011114.2:c.1218T>A	XP_016866603.1:p.Asp406Glu
XM_017011119.2:c.948T>A	XP_016866608.1:p.Asp316Glu
XM_017011122.1:c.870T>A	XP_016866611.1:p.Asp290Glu
XR_001743536.1:n.1729T>A
XR_001743538.1:n.1729T>A
XR_942529.2:n.1729T>A
NM_020771.4:c.1452T>A MANE Select	NP_065822.2:p.Asp484Glu
NM_001321080.2:c.1320T>A	NP_001308009.1:p.Asp440Glu
NM_001321083.2:c.1350T>A	NP_001308012.1:p.Asp450Glu
NM_001321084.2:c.948T>A	NP_001308013.1:p.Asp316Glu
NM_001350554.2:c.1218T>A	NP_001337483.1:p.Asp406Glu
NM_001350555.2:c.1161T>A	NP_001337484.1:p.Asp387Glu
NM_001350556.2:c.966T>A	NP_001337485.1:p.Asp322Glu
NM_001350557.2:c.948T>A	NP_001337486.1:p.Asp316Glu
NM_001350558.2:c.948T>A	NP_001337487.1:p.Asp316Glu
NM_001350559.2:c.870T>A	NP_001337488.1:p.Asp290Glu
NM_001350560.2:c.669T>A	NP_001337489.1:p.Asp223Glu
NR_104424.2:n.1823T>A
NR_146787.2:n.1570T>A
NR_146788.2:n.1740T>A
NR_146789.2:n.1729T>A
NR_146790.2:n.1729T>A
NR_146791.2:n.1729T>A
NR_146792.2:n.1823T>A