Canonical Allele Identifier: CA376729957

Gene: CHAT

Linked Data

• COSMIC: COSM1348104 ; COSM5157830
• MyVariant Identifiers: chr10:g.50833587A>G (hg19) ; chr10:g.49625541A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49625541A>G , CM000672.2:g.49625541A>G	GRCh38
NC_000010.10:g.50833587A>G , CM000672.1:g.50833587A>G	GRCh37
NC_000010.9:g.50503593A>G	NCBI36
NG_011797.1:g.21447A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337653.7:c.821A>G MANE Select	ENSP00000337103.2:p.Tyr274Cys
ENST00000337653.6:c.821A>G	ENSP00000337103.2:p.Tyr274Cys
ENST00000339797.5:c.467A>G	ENSP00000343486.1:p.Tyr156Cys
ENST00000351556.7:c.467A>G	ENSP00000345878.3:p.Tyr156Cys
ENST00000395559.6:c.467A>G	ENSP00000378926.2:p.Tyr156Cys
ENST00000395562.2:c.575A>G	ENSP00000378929.2:p.Tyr192Cys
ENST00000466590.6:c.*552A>G	ENSP00000473443.1:n.*552A>G
NM_001142929.1:c.467A>G	NP_001136401.1:p.Tyr156Cys
NM_001142933.1:c.575A>G	NP_001136405.1:p.Tyr192Cys
NM_001142934.1:c.467A>G	NP_001136406.1:p.Tyr156Cys
NM_020549.4:c.821A>G	NP_065574.3:p.Tyr274Cys
NM_020984.3:c.467A>G	NP_066264.3:p.Tyr156Cys
NM_020985.3:c.467A>G	NP_066265.3:p.Tyr156Cys
NM_020986.3:c.467A>G	NP_066266.3:p.Tyr156Cys
NM_001142929.2:c.467A>G	NP_001136401.2:p.Tyr156Cys
NM_001142933.2:c.575A>G	NP_001136405.2:p.Tyr192Cys
NM_001142934.2:c.467A>G	NP_001136406.2:p.Tyr156Cys
NM_020549.5:c.821A>G MANE Select	NP_065574.4:p.Tyr274Cys
NM_020984.4:c.467A>G	NP_066264.4:p.Tyr156Cys
NM_020985.4:c.467A>G	NP_066265.4:p.Tyr156Cys
NM_020986.4:c.467A>G	NP_066266.4:p.Tyr156Cys