Canonical Allele Identifier: CA2671694018
Gene: HADH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108027784A>G , CM000666.2:g.108027784A>G GRCh38
NC_000004.11:g.108948940A>G , CM000666.1:g.108948940A>G GRCh37
NC_000004.10:g.109168389A>G NCBI36
NG_008156.2:g.43001A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507260.3:n.4943A>G
ENST00000510728.6:n.1697+24A>G
ENST00000514776.3:n.166A>G
ENST00000515462.7:n.1920A>G
ENST00000626637.2:c.721+24A>G ENSP00000486771.1:n.721+24A>G
ENST00000638648.2:c.721+24A>G ENSP00000507949.1:n.721+24A>G
ENST00000640201.2:n.819A>G
ENST00000640752.2:n.4919+24A>G
ENST00000682067.1:c.542+24A>G
ENST00000682086.1:n.802A>G
ENST00000682373.1:c.368+24A>G
ENST00000684696.1:c.637-155A>G ENSP00000507675.1:n.637-155A>G
ENST00000309522.8:c.709+24A>G MANE Select ENSP00000312288.4:n.709+24A>G
ENST00000403312.6:c.709+24A>G ENSP00000385638.3:n.709+24A>G
ENST00000505878.4:c.886+24A>G ENSP00000425952.2:n.886+24A>G
ENST00000514776.2:n.166A>G
ENST00000515462.6:n.1920A>G
ENST00000638559.1:c.567+24A>G
ENST00000638621.1:c.295+24A>G ENSP00000491581.1:n.295+24A>G
ENST00000638648.1:n.860+24A>G
ENST00000639146.1:c.709+24A>G ENSP00000492345.1:n.709+24A>G
ENST00000639335.1:c.*144+24A>G ENSP00000491310.1:n.*144+24A>G
ENST00000639698.1:c.516+4221A>G ENSP00000492420.1:n.516+4221A>G
ENST00000639784.1:c.373+4221A>G
ENST00000640048.1:c.681+24A>G ENSP00000492009.1:n.681+24A>G
ENST00000640060.1:c.*804+24A>G ENSP00000492734.1:n.*804+24A>G
ENST00000640201.1:n.688A>G
ENST00000640752.1:n.4912+24A>G
ENST00000309522.7:c.709+24A>G ENSP00000312288.3:n.709+24A>G
ENST00000403312.5:c.886+24A>G ENSP00000385638.2:n.886+24A>G
ENST00000505878.3:c.721+24A>G ENSP00000425952.1:n.721+24A>G
ENST00000507260.1:n.433A>G
ENST00000510728.5:n.249+24A>G
ENST00000515462.5:n.70A>G
ENST00000603302.5:c.709+24A>G ENSP00000474560.1:n.709+24A>G
ENST00000626637.1:c.721+24A>G ENSP00000486771.1:n.721+24A>G
NM_001184705.2:c.709+24A>G NP_001171634.2:n.709+24A>G
NM_005327.4:c.709+24A>G NP_005318.3:n.709+24A>G
XM_005262972.1:c.721+24A>G XP_005263029.1:n.721+24A>G
XR_938726.1:n.882A>G
NM_001331027.1:c.721+24A>G NP_001317956.1:n.721+24A>G
XR_001741214.2:n.803+24A>G
XR_002959727.1:n.827A>G
NM_001184705.3:c.709+24A>G NP_001171634.2:n.709+24A>G
NM_005327.7:c.709+24A>G MANE Select NP_005318.6:n.709+24A>G
NM_001184705.4:c.709+24A>G NP_001171634.3:n.709+24A>G
NM_001331027.2:c.721+24A>G NP_001317956.2:n.721+24A>G