Canonical Allele Identifier: CA1908795077

Gene: SLC18A3 CHAT

Linked Data

• dbSNP Id: rs1838310011

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49611949_49611951del , CM000672.2:g.49611949_49611951del	GRCh38
NC_000010.10:g.50819995_50819997del , CM000672.1:g.50819995_50819997del	GRCh37
NC_000010.9:g.50490001_50490003del	NCBI36
NG_011797.1:g.7855_7857del
NG_053144.1:g.6649_6651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374115.5:c.1209_1211del (SLC18A3) MANE Select	ENSP00000363229.3:p.Thr404del
ENST00000339797.5:c.-69+2750_-69+2752del (CHAT)	ENSP00000343486.1:n.-69+2750_-69+2752del
ENST00000374115.4:c.1209_1211del (SLC18A3)	ENSP00000363229.3:p.Thr404del
NM_003055.2:c.1209_1211del (SLC18A3)	NP_003046.2:p.Thr404del
NM_020984.3:c.-69+2750_-69+2752del (CHAT)	NP_066264.3:n.-69+2750_-69+2752del
NM_003055.3:c.1209_1211del (SLC18A3) MANE Select	NP_003046.2:p.Thr404del
NM_020984.4:c.-69+2750_-69+2752del (CHAT)	NP_066264.4:n.-69+2750_-69+2752del