Canonical Allele Identifier: CA2396125809

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19963715G= , CM000684.2:g.19963715G=	GRCh38
NC_000022.10:g.19951238G= , CM000684.1:g.19951238G=	GRCh37
NC_000022.9:g.18331238G=	NCBI36
NG_011526.1:g.26976G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.439G= MANE Select	ENSP00000354511.6:p.Ala147=
ENST00000428707.2:c.439G=	ENSP00000387695.2:p.Ala147=
ENST00000676678.1:c.439G=	ENSP00000503719.1:p.Ala147=
ENST00000677397.1:c.289G=	ENSP00000503422.1:p.Ala97=
ENST00000677564.1:n.222G=
ENST00000677675.1:n.239G=
ENST00000678240.1:n.287G=
ENST00000678255.1:c.439G=	ENSP00000504402.1:p.Ala147=
ENST00000678769.1:c.439G=	ENSP00000503289.1:p.Ala147=
ENST00000678868.1:c.439G=	ENSP00000503583.1:p.Ala147=
ENST00000678945.1:n.249G=
ENST00000207636.9:c.439G=	ENSP00000207636.5:p.Ala147=
ENST00000361682.10:c.439G=	ENSP00000354511.6:p.Ala147=
ENST00000403184.5:c.439G=	ENSP00000383966.1:p.Ala147=
ENST00000403710.5:c.439G=	ENSP00000385917.1:p.Ala147=
ENST00000406520.7:c.439G=	ENSP00000385150.3:p.Ala147=
ENST00000407537.5:c.439G=	ENSP00000384654.2:p.Ala147=
ENST00000412786.5:c.439G=	ENSP00000403958.1:p.Ala147=
ENST00000428707.1:c.17G=
ENST00000449653.5:c.289G=	ENSP00000416778.1:p.Ala97=
ENST00000493893.1:n.177G=
NM_000754.3:c.439G=	NP_000745.1:p.Ala147=
NM_001135161.1:c.439G=	NP_001128633.1:p.Ala147=
NM_001135162.1:c.439G=	NP_001128634.1:p.Ala147=
NM_007310.2:c.289G=	NP_009294.1:p.Ala97=
XM_011529885.1:c.553G=	XP_011528187.1:p.Ala185=
XM_011529886.1:c.553G=	XP_011528188.1:p.Ala185=
XM_011529887.1:c.439G=	XP_011528189.1:p.Ala147=
XM_011529888.1:c.439G=	XP_011528190.1:p.Ala147=
XM_011529889.1:c.439G=	XP_011528191.1:p.Ala147=
XM_011529890.1:c.439G=	XP_011528192.1:p.Ala147=
XM_011529891.1:c.439G=	XP_011528193.1:p.Ala147=
NM_001362828.1:c.439G=	NP_001349757.1:p.Ala147=
XM_011529886.2:c.850G=	XP_011528188.2:p.Ala284=
XM_017028595.1:c.439G=	XP_016884084.1:p.Ala147=
NM_000754.4:c.439G= MANE Select	NP_000745.1:p.Ala147=
NM_001135161.2:c.439G=	NP_001128633.1:p.Ala147=
NM_001135162.2:c.439G=	NP_001128634.1:p.Ala147=
NM_001362828.2:c.439G=	NP_001349757.1:p.Ala147=
NM_007310.3:c.289G=	NP_009294.1:p.Ala97=