Canonical Allele Identifier: CA915952703

Gene: COMT ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19969895G>T , CM000684.2:g.19969895G>T	GRCh38
NC_000022.10:g.19957418G>T , CM000684.1:g.19957418G>T	GRCh37
NC_000022.9:g.18337418G>T	NCBI36
NG_011526.1:g.33156G>T
NG_023326.1:g.51892C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.*1159G>T (COMT) MANE Select	ENSP00000354511.6:n.*1159G>T
ENST00000677564.1:n.1758G>T (COMT)
ENST00000678255.1:c.*1159G>T (COMT)	ENSP00000504402.1:n.*1159G>T
ENST00000678868.1:c.*1159G>T (COMT)	ENSP00000503583.1:n.*1159G>T
ENST00000678945.1:n.1843G>T (COMT)
ENST00000361682.10:c.*1159G>T (COMT)	ENSP00000354511.6:n.*1159G>T
NM_000754.3:c.*1159G>T (COMT)	NP_000745.1:n.*1159G>T
NM_001135161.1:c.*1159G>T (COMT)	NP_001128633.1:n.*1159G>T
NM_001135162.1:c.*1159G>T (COMT)	NP_001128634.1:n.*1159G>T
NM_001670.2:c.*861C>A (ARVCF)	NP_001661.1:n.*861C>A
NM_007310.2:c.*1159G>T (COMT)	NP_009294.1:n.*1159G>T
XM_005261242.1:c.2763+1991C>A (ARVCF)	XP_005261299.1:n.2763+1991C>A
XM_005261243.3:c.*861C>A (ARVCF)	XP_005261300.1:n.*861C>A
XM_005261244.3:c.*822C>A (ARVCF)	XP_005261301.1:n.*822C>A
XM_006724243.1:c.2781+1991C>A (ARVCF)	XP_006724306.1:n.2781+1991C>A
XM_006724245.2:c.*822C>A (ARVCF)	XP_006724308.1:n.*822C>A
XM_006724246.2:c.2535+1991C>A (ARVCF)	XP_006724309.1:n.2535+1991C>A
XM_006724247.2:c.*861C>A (ARVCF)	XP_006724310.1:n.*861C>A
XM_006724248.2:c.*861C>A (ARVCF)	XP_006724311.1:n.*861C>A
XM_011530179.1:c.2748+1991C>A (ARVCF)	XP_011528481.1:n.2748+1991C>A
XM_011530182.1:c.1347+1991C>A (ARVCF)	XP_011528484.1:n.1347+1991C>A
XM_011530183.1:c.*822C>A (ARVCF)	XP_011528485.1:n.*822C>A
XR_937863.1:n.3717C>A (ARVCF)
NM_001362828.1:c.*1159G>T (COMT)	NP_001349757.1:n.*1159G>T
XM_005261242.3:c.2763+1991C>A (ARVCF)	XP_005261299.1:n.2763+1991C>A
XM_006724243.3:c.2781+1991C>A (ARVCF)	XP_006724306.1:n.2781+1991C>A
XM_006724246.4:c.2535+1991C>A (ARVCF)	XP_006724309.1:n.2535+1991C>A
XM_011530179.3:c.2748+1991C>A (ARVCF)	XP_011528481.1:n.2748+1991C>A
XM_011530182.3:c.1347+1991C>A (ARVCF)	XP_011528484.1:n.1347+1991C>A
XM_024452249.1:c.2535+1991C>A (ARVCF)	XP_024308017.1:n.2535+1991C>A
NM_000754.4:c.*1159G>T (COMT) MANE Select	NP_000745.1:n.*1159G>T
NM_001135161.2:c.*1159G>T (COMT)	NP_001128633.1:n.*1159G>T
NM_001135162.2:c.*1159G>T (COMT)	NP_001128634.1:n.*1159G>T
NM_001362828.2:c.*1159G>T (COMT)	NP_001349757.1:n.*1159G>T
NM_007310.3:c.*1159G>T (COMT)	NP_009294.1:n.*1159G>T