Canonical Allele Identifier: CA2396118934

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19950097_19950099delinsGTT , CM000684.2:g.19950097_19950099delinsGTT	GRCh38
NC_000022.10:g.19937620_19937622delinsGTT , CM000684.1:g.19937620_19937622delinsGTT	GRCh37
NC_000022.9:g.18317620_18317622delinsGTT	NCBI36
NG_011526.1:g.13358_13360delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.-92+8200_-92+8202delinsGTT MANE Select	ENSP00000354511.6:n.-92+8200_-92+8202delinsGTT
ENST00000428707.2:c.-92+8200_-92+8202delinsGTT	ENSP00000387695.2:n.-92+8200_-92+8202delinsGTT
ENST00000676678.1:c.-92+8522_-92+8524delinsGTT	ENSP00000503719.1:n.-92+8522_-92+8524delinsGTT
ENST00000678769.1:c.-92+8200_-92+8202delinsGTT	ENSP00000503289.1:n.-92+8200_-92+8202delinsGTT
ENST00000678868.1:c.-92+2607_-92+2609delinsGTT	ENSP00000503583.1:n.-92+2607_-92+2609delinsGTT
ENST00000361682.10:c.-92+8200_-92+8202delinsGTT	ENSP00000354511.6:n.-92+8200_-92+8202delinsGTT
ENST00000403184.5:c.-92+8200_-92+8202delinsGTT	ENSP00000383966.1:n.-92+8200_-92+8202delinsGTT
ENST00000403710.5:c.-386+8200_-386+8202delinsGTT	ENSP00000385917.1:n.-386+8200_-386+8202delinsGTT
ENST00000407537.5:c.-270+8200_-270+8202delinsGTT	ENSP00000384654.2:n.-270+8200_-270+8202delinsGTT
ENST00000467943.5:n.105+8200_105+8202delinsGTT
NM_000754.3:c.-92+8200_-92+8202delinsGTT	NP_000745.1:n.-92+8200_-92+8202delinsGTT
XM_011529887.1:c.-92+8200_-92+8202delinsGTT	XP_011528189.1:n.-92+8200_-92+8202delinsGTT
XM_011529890.1:c.-386+8200_-386+8202delinsGTT	XP_011528192.1:n.-386+8200_-386+8202delinsGTT
XM_011529891.1:c.-386+7922_-386+7924delinsGTT	XP_011528193.1:n.-386+7922_-386+7924delinsGTT
NM_001362828.1:c.-386+8200_-386+8202delinsGTT	NP_001349757.1:n.-386+8200_-386+8202delinsGTT
XM_017028595.1:c.-386+7922_-386+7924delinsGTT	XP_016884084.1:n.-386+7922_-386+7924delinsGTT
NM_000754.4:c.-92+8200_-92+8202delinsGTT MANE Select	NP_000745.1:n.-92+8200_-92+8202delinsGTT
NM_001362828.2:c.-386+8200_-386+8202delinsGTT	NP_001349757.1:n.-386+8200_-386+8202delinsGTT