Canonical Allele Identifier: CA2001382887

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910195_113910199delinsGCTTT , CM000673.2:g.113910195_113910199delinsGCTTT	GRCh38
NC_000011.9:g.113780917_113780921delinsGCTTT , CM000673.1:g.113780917_113780921delinsGCTTT	GRCh37
NC_000011.8:g.113286127_113286131delinsGCTTT	NCBI36
NG_011483.1:g.10329_10333delinsGCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.213+740_213+744delinsGCTTT MANE Select	ENSP00000260191.2:n.213+740_213+744delins...
ENST00000260191.7:c.213+740_213+744delinsGCTTT	ENSP00000260191.2:n.213+740_213+744delins...
ENST00000260191.6:c.213+740_213+744delinsGCTTT	ENSP00000260191.2:n.213+740_213+744delins...
ENST00000537778.5:c.180+740_180+744delinsGCTTT	ENSP00000443118.1:n.180+740_180+744delins...
NM_006028.4:c.213+740_213+744delinsGCTTT	NP_006019.1:n.213+740_213+744delinsGCTTT
XM_011543063.1:c.180+740_180+744delinsGCTTT	XP_011541365.1:n.180+740_180+744delinsGCT...
XM_011543064.1:c.12+11112_12+11116delinsGCTTT	XP_011541366.1:n.12+11112_12+11116delinsG...
XM_011543066.1:c.180+740_180+744delinsGCTTT	XP_011541368.1:n.180+740_180+744delinsGCT...
NM_001363563.1:c.180+740_180+744delinsGCTTT	NP_001350492.1:n.180+740_180+744delinsGCT...
XM_024448767.1:c.-82+740_-82+744delinsGCTTT	XP_024304535.1:n.-82+740_-82+744delinsGCT...
XR_001748034.2:n.464+740_464+744delinsGCTTT
NM_001363563.2:c.180+740_180+744delinsGCTTT	NP_001350492.1:n.180+740_180+744delinsGCT...
NM_006028.5:c.213+740_213+744delinsGCTTT MANE Select	NP_006019.1:n.213+740_213+744delinsGCTTT