Canonical Allele Identifier: CA376748058

Gene: CHAT

Linked Data

• dbSNP Id: rs1564493736
• gnomAD v4: 10-49655214-C-T
• MyVariant Identifiers: chr10:g.50863260C>T (hg19) ; chr10:g.49655214C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49655214C>T , CM000672.2:g.49655214C>T	GRCh38
NC_000010.10:g.50863260C>T , CM000672.1:g.50863260C>T	GRCh37
NC_000010.9:g.50533266C>T	NCBI36
NG_011797.1:g.51120C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337653.7:c.1754C>T MANE Select	ENSP00000337103.2:p.Thr585Ile
ENST00000638282.1:c.*591C>T	ENSP00000492646.1:n.*591C>T
ENST00000638683.1:n.391C>T
ENST00000640822.1:c.617C>T	ENSP00000491328.1:p.Thr206Ile
ENST00000337653.6:c.1754C>T	ENSP00000337103.2:p.Thr585Ile
ENST00000339797.5:c.1400C>T	ENSP00000343486.1:p.Thr467Ile
ENST00000351556.7:c.1400C>T	ENSP00000345878.3:p.Thr467Ile
ENST00000395559.6:c.1400C>T	ENSP00000378926.2:p.Thr467Ile
ENST00000395562.2:c.1508C>T	ENSP00000378929.2:p.Thr503Ile
ENST00000466590.6:c.*1485C>T	ENSP00000473443.1:n.*1485C>T
NM_001142929.1:c.1400C>T	NP_001136401.1:p.Thr467Ile
NM_001142933.1:c.1508C>T	NP_001136405.1:p.Thr503Ile
NM_001142934.1:c.1400C>T	NP_001136406.1:p.Thr467Ile
NM_020549.4:c.1754C>T	NP_065574.3:p.Thr585Ile
NM_020984.3:c.1400C>T	NP_066264.3:p.Thr467Ile
NM_020985.3:c.1400C>T	NP_066265.3:p.Thr467Ile
NM_020986.3:c.1400C>T	NP_066266.3:p.Thr467Ile
NM_001142929.2:c.1400C>T	NP_001136401.2:p.Thr467Ile
NM_001142933.2:c.1508C>T	NP_001136405.2:p.Thr503Ile
NM_001142934.2:c.1400C>T	NP_001136406.2:p.Thr467Ile
NM_020549.5:c.1754C>T MANE Select	NP_065574.4:p.Thr585Ile
NM_020984.4:c.1400C>T	NP_066264.4:p.Thr467Ile
NM_020985.4:c.1400C>T	NP_066265.4:p.Thr467Ile
NM_020986.4:c.1400C>T	NP_066266.4:p.Thr467Ile