Canonical Allele Identifier: CA2655336245

Gene: COMT ARVCF

Linked Data

• gnomAD v4: 22-19968739-G-GCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19968744_19968746dup , CM000684.2:g.19968744_19968746dup	GRCh38
NC_000022.10:g.19956267_19956269dup , CM000684.1:g.19956267_19956269dup	GRCh37
NC_000022.9:g.18336267_18336269dup	NCBI36
NG_011526.1:g.32005_32007dup
NG_023326.1:g.53045_53047dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.*8_*10dup (COMT) MANE Select	ENSP00000354511.6:n.*8_*10dup
ENST00000428707.2:c.*1317_*1319dup (COMT)	ENSP00000387695.2:n.*1317_*1319dup
ENST00000676678.1:c.*8_*10dup (COMT)	ENSP00000503719.1:n.*8_*10dup
ENST00000677397.1:c.*403_*405dup (COMT)	ENSP00000503422.1:n.*403_*405dup
ENST00000677470.1:n.674_676dup (COMT)
ENST00000677564.1:n.607_609dup (COMT)
ENST00000677675.1:n.624_626dup (COMT)
ENST00000678255.1:c.*8_*10dup (COMT)	ENSP00000504402.1:n.*8_*10dup
ENST00000678769.1:c.*8_*10dup (COMT)	ENSP00000503289.1:n.*8_*10dup
ENST00000678868.1:c.*8_*10dup (COMT)	ENSP00000503583.1:n.*8_*10dup
ENST00000678945.1:n.692_694dup (COMT)
ENST00000207636.9:c.*282_*284dup (COMT)	ENSP00000207636.5:n.*282_*284dup
ENST00000361682.10:c.*8_*10dup (COMT)	ENSP00000354511.6:n.*8_*10dup
ENST00000403710.5:c.*8_*10dup (COMT)	ENSP00000385917.1:n.*8_*10dup
ENST00000406520.7:c.*8_*10dup (COMT)	ENSP00000385150.3:n.*8_*10dup
ENST00000407537.5:c.*8_*10dup (COMT)	ENSP00000384654.2:n.*8_*10dup
ENST00000449653.5:c.*8_*10dup (COMT)	ENSP00000416778.1:n.*8_*10dup
NM_000754.3:c.*8_*10dup (COMT)	NP_000745.1:n.*8_*10dup
NM_001135161.1:c.*8_*10dup (COMT)	NP_001128633.1:n.*8_*10dup
NM_001135162.1:c.*8_*10dup (COMT)	NP_001128634.1:n.*8_*10dup
NM_007310.2:c.*8_*10dup (COMT)	NP_009294.1:n.*8_*10dup
XM_005261242.1:c.2764-1533_2764-1531dup (ARVCF)	XP_005261299.1:n.2764-1533_2764-1531dup
XM_006724243.1:c.2782-1533_2782-1531dup (ARVCF)	XP_006724306.1:n.2782-1533_2782-1531dup
XM_006724246.2:c.2536-1533_2536-1531dup (ARVCF)	XP_006724309.1:n.2536-1533_2536-1531dup
XM_011529886.1:c.*8_*10dup (COMT)	XP_011528188.1:n.*8_*10dup
XM_011530179.1:c.2749-1533_2749-1531dup (ARVCF)	XP_011528481.1:n.2749-1533_2749-1531dup
XM_011530182.1:c.1348-1533_1348-1531dup (ARVCF)	XP_011528484.1:n.1348-1533_1348-1531dup
NM_001362828.1:c.*8_*10dup (COMT)	NP_001349757.1:n.*8_*10dup
XM_005261242.3:c.2764-1533_2764-1531dup (ARVCF)	XP_005261299.1:n.2764-1533_2764-1531dup
XM_006724243.3:c.2782-1533_2782-1531dup (ARVCF)	XP_006724306.1:n.2782-1533_2782-1531dup
XM_006724246.4:c.2536-1533_2536-1531dup (ARVCF)	XP_006724309.1:n.2536-1533_2536-1531dup
XM_011529886.2:c.*8_*10dup (COMT)	XP_011528188.2:n.*8_*10dup
XM_011530179.3:c.2749-1533_2749-1531dup (ARVCF)	XP_011528481.1:n.2749-1533_2749-1531dup
XM_011530182.3:c.1348-1533_1348-1531dup (ARVCF)	XP_011528484.1:n.1348-1533_1348-1531dup
XM_017028595.1:c.*8_*10dup (COMT)	XP_016884084.1:n.*8_*10dup
XM_024452249.1:c.2536-1533_2536-1531dup (ARVCF)	XP_024308017.1:n.2536-1533_2536-1531dup
NM_000754.4:c.*8_*10dup (COMT) MANE Select	NP_000745.1:n.*8_*10dup
NM_001135161.2:c.*8_*10dup (COMT)	NP_001128633.1:n.*8_*10dup
NM_001135162.2:c.*8_*10dup (COMT)	NP_001128634.1:n.*8_*10dup
NM_001362828.2:c.*8_*10dup (COMT)	NP_001349757.1:n.*8_*10dup
NM_007310.3:c.*8_*10dup (COMT)	NP_009294.1:n.*8_*10dup