Canonical Allele Identifier: CA469605662

Gene: CHAT

Linked Data

• MyVariant Identifiers: chr10:g.50863186C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49655140C>G , CM000672.2:g.49655140C>G	GRCh38
NC_000010.10:g.50863186C>G , CM000672.1:g.50863186C>G	GRCh37
NC_000010.9:g.50533192C>G	NCBI36
NG_011797.1:g.51046C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000337653.7:c.1680C>G MANE Select	ENSP00000337103.2:p.Arg560=
ENST00000638282.1:c.*517C>G	ENSP00000492646.1:n.*517C>G
ENST00000638683.1:n.317C>G
ENST00000640822.1:c.543C>G	ENSP00000491328.1:p.Arg181=
ENST00000337653.6:c.1680C>G	ENSP00000337103.2:p.Arg560=
ENST00000339797.5:c.1326C>G	ENSP00000343486.1:p.Arg442=
ENST00000351556.7:c.1326C>G	ENSP00000345878.3:p.Arg442=
ENST00000395559.6:c.1326C>G	ENSP00000378926.2:p.Arg442=
ENST00000395562.2:c.1434C>G	ENSP00000378929.2:p.Arg478=
ENST00000466590.6:c.*1411C>G	ENSP00000473443.1:n.*1411C>G
NM_001142929.1:c.1326C>G	NP_001136401.1:p.Arg442=
NM_001142933.1:c.1434C>G	NP_001136405.1:p.Arg478=
NM_001142934.1:c.1326C>G	NP_001136406.1:p.Arg442=
NM_020549.4:c.1680C>G	NP_065574.3:p.Arg560=
NM_020984.3:c.1326C>G	NP_066264.3:p.Arg442=
NM_020985.3:c.1326C>G	NP_066265.3:p.Arg442=
NM_020986.3:c.1326C>G	NP_066266.3:p.Arg442=
NM_001142929.2:c.1326C>G	NP_001136401.2:p.Arg442=
NM_001142933.2:c.1434C>G	NP_001136405.2:p.Arg478=
NM_001142934.2:c.1326C>G	NP_001136406.2:p.Arg442=
NM_020549.5:c.1680C>G MANE Select	NP_065574.4:p.Arg560=
NM_020984.4:c.1326C>G	NP_066264.4:p.Arg442=
NM_020985.4:c.1326C>G	NP_066265.4:p.Arg442=
NM_020986.4:c.1326C>G	NP_066266.4:p.Arg442=