Canonical Allele Identifier: CA376729963
Gene: CHAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49625542T>A , CM000672.2:g.49625542T>A GRCh38
NC_000010.10:g.50833588T>A , CM000672.1:g.50833588T>A GRCh37
NC_000010.9:g.50503594T>A NCBI36
NG_011797.1:g.21448T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000337653.7:c.822T>A MANE Select ENSP00000337103.2:p.Tyr274Ter
ENST00000337653.6:c.822T>A ENSP00000337103.2:p.Tyr274Ter
ENST00000339797.5:c.468T>A ENSP00000343486.1:p.Tyr156Ter
ENST00000351556.7:c.468T>A ENSP00000345878.3:p.Tyr156Ter
ENST00000395559.6:c.468T>A ENSP00000378926.2:p.Tyr156Ter
ENST00000395562.2:c.576T>A ENSP00000378929.2:p.Tyr192Ter
ENST00000466590.6:c.*553T>A ENSP00000473443.1:n.*553T>A
NM_001142929.1:c.468T>A NP_001136401.1:p.Tyr156Ter
NM_001142933.1:c.576T>A NP_001136405.1:p.Tyr192Ter
NM_001142934.1:c.468T>A NP_001136406.1:p.Tyr156Ter
NM_020549.4:c.822T>A NP_065574.3:p.Tyr274Ter
NM_020984.3:c.468T>A NP_066264.3:p.Tyr156Ter
NM_020985.3:c.468T>A NP_066265.3:p.Tyr156Ter
NM_020986.3:c.468T>A NP_066266.3:p.Tyr156Ter
NM_001142929.2:c.468T>A NP_001136401.2:p.Tyr156Ter
NM_001142933.2:c.576T>A NP_001136405.2:p.Tyr192Ter
NM_001142934.2:c.468T>A NP_001136406.2:p.Tyr156Ter
NM_020549.5:c.822T>A MANE Select NP_065574.4:p.Tyr274Ter
NM_020984.4:c.468T>A NP_066264.4:p.Tyr156Ter
NM_020985.4:c.468T>A NP_066265.4:p.Tyr156Ter
NM_020986.4:c.468T>A NP_066266.4:p.Tyr156Ter