Canonical Allele Identifier: CA376747718

Gene: CHAT

Linked Data

• dbSNP Id: rs1839995550
• MyVariant Identifiers: chr10:g.50863223G>A (hg19) ; chr10:g.49655177G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49655177G>A , CM000672.2:g.49655177G>A	GRCh38
NC_000010.10:g.50863223G>A , CM000672.1:g.50863223G>A	GRCh37
NC_000010.9:g.50533229G>A	NCBI36
NG_011797.1:g.51083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337653.7:c.1717G>A MANE Select	ENSP00000337103.2:p.Ala573Thr
ENST00000638282.1:c.*554G>A	ENSP00000492646.1:n.*554G>A
ENST00000638683.1:n.354G>A
ENST00000640822.1:c.580G>A	ENSP00000491328.1:p.Ala194Thr
ENST00000337653.6:c.1717G>A	ENSP00000337103.2:p.Ala573Thr
ENST00000339797.5:c.1363G>A	ENSP00000343486.1:p.Ala455Thr
ENST00000351556.7:c.1363G>A	ENSP00000345878.3:p.Ala455Thr
ENST00000395559.6:c.1363G>A	ENSP00000378926.2:p.Ala455Thr
ENST00000395562.2:c.1471G>A	ENSP00000378929.2:p.Ala491Thr
ENST00000466590.6:c.*1448G>A	ENSP00000473443.1:n.*1448G>A
NM_001142929.1:c.1363G>A	NP_001136401.1:p.Ala455Thr
NM_001142933.1:c.1471G>A	NP_001136405.1:p.Ala491Thr
NM_001142934.1:c.1363G>A	NP_001136406.1:p.Ala455Thr
NM_020549.4:c.1717G>A	NP_065574.3:p.Ala573Thr
NM_020984.3:c.1363G>A	NP_066264.3:p.Ala455Thr
NM_020985.3:c.1363G>A	NP_066265.3:p.Ala455Thr
NM_020986.3:c.1363G>A	NP_066266.3:p.Ala455Thr
NM_001142929.2:c.1363G>A	NP_001136401.2:p.Ala455Thr
NM_001142933.2:c.1471G>A	NP_001136405.2:p.Ala491Thr
NM_001142934.2:c.1363G>A	NP_001136406.2:p.Ala455Thr
NM_020549.5:c.1717G>A MANE Select	NP_065574.4:p.Ala573Thr
NM_020984.4:c.1363G>A	NP_066264.4:p.Ala455Thr
NM_020985.4:c.1363G>A	NP_066265.4:p.Ala455Thr
NM_020986.4:c.1363G>A	NP_066266.4:p.Ala455Thr