Canonical Allele Identifier: CA376721778

Gene: SLC18A3 CHAT

Linked Data

• dbSNP Id: rs1564466634
• MyVariant Identifiers: chr10:g.50819802T>C (hg19) ; chr10:g.49611756T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49611756T>C , CM000672.2:g.49611756T>C	GRCh38
NC_000010.10:g.50819802T>C , CM000672.1:g.50819802T>C	GRCh37
NC_000010.9:g.50489808T>C	NCBI36
NG_011797.1:g.7662T>C
NG_053144.1:g.6456T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374115.5:c.1016T>C (SLC18A3) MANE Select	ENSP00000363229.3:p.Val339Ala
ENST00000339797.5:c.-69+2557T>C (CHAT)	ENSP00000343486.1:n.-69+2557T>C
ENST00000374115.4:c.1016T>C (SLC18A3)	ENSP00000363229.3:p.Val339Ala
NM_003055.2:c.1016T>C (SLC18A3)	NP_003046.2:p.Val339Ala
NM_020984.3:c.-69+2557T>C (CHAT)	NP_066264.3:n.-69+2557T>C
NM_003055.3:c.1016T>C (SLC18A3) MANE Select	NP_003046.2:p.Val339Ala
NM_020984.4:c.-69+2557T>C (CHAT)	NP_066264.4:n.-69+2557T>C