Canonical Allele Identifier: CA376729971

Gene: CHAT

Linked Data

• MyVariant Identifiers: chr10:g.50833589G>T (hg19) ; chr10:g.49625543G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49625543G>T , CM000672.2:g.49625543G>T	GRCh38
NC_000010.10:g.50833589G>T , CM000672.1:g.50833589G>T	GRCh37
NC_000010.9:g.50503595G>T	NCBI36
NG_011797.1:g.21449G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337653.7:c.823G>T MANE Select	ENSP00000337103.2:p.Gly275Trp
ENST00000337653.6:c.823G>T	ENSP00000337103.2:p.Gly275Trp
ENST00000339797.5:c.469G>T	ENSP00000343486.1:p.Gly157Trp
ENST00000351556.7:c.469G>T	ENSP00000345878.3:p.Gly157Trp
ENST00000395559.6:c.469G>T	ENSP00000378926.2:p.Gly157Trp
ENST00000395562.2:c.577G>T	ENSP00000378929.2:p.Gly193Trp
ENST00000466590.6:c.*554G>T	ENSP00000473443.1:n.*554G>T
NM_001142929.1:c.469G>T	NP_001136401.1:p.Gly157Trp
NM_001142933.1:c.577G>T	NP_001136405.1:p.Gly193Trp
NM_001142934.1:c.469G>T	NP_001136406.1:p.Gly157Trp
NM_020549.4:c.823G>T	NP_065574.3:p.Gly275Trp
NM_020984.3:c.469G>T	NP_066264.3:p.Gly157Trp
NM_020985.3:c.469G>T	NP_066265.3:p.Gly157Trp
NM_020986.3:c.469G>T	NP_066266.3:p.Gly157Trp
NM_001142929.2:c.469G>T	NP_001136401.2:p.Gly157Trp
NM_001142933.2:c.577G>T	NP_001136405.2:p.Gly193Trp
NM_001142934.2:c.469G>T	NP_001136406.2:p.Gly157Trp
NM_020549.5:c.823G>T MANE Select	NP_065574.4:p.Gly275Trp
NM_020984.4:c.469G>T	NP_066264.4:p.Gly157Trp
NM_020985.4:c.469G>T	NP_066265.4:p.Gly157Trp
NM_020986.4:c.469G>T	NP_066266.4:p.Gly157Trp