Canonical Allele Identifier: CA1908834650
Gene: CHAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49655134C= , CM000672.2:g.49655134C= GRCh38
NC_000010.10:g.50863180C= , CM000672.1:g.50863180C= GRCh37
NC_000010.9:g.50533186C= NCBI36
NG_011797.1:g.51040C=

Transcript Alleles

HGVS Amino-acid change
ENST00000337653.7:c.1674C= MANE Select ENSP00000337103.2:p.Ser558=
ENST00000638282.1:c.*511C= ENSP00000492646.1:n.*511C=
ENST00000638683.1:n.311C=
ENST00000640822.1:c.537C= ENSP00000491328.1:p.Ser179=
ENST00000337653.6:c.1674C= ENSP00000337103.2:p.Ser558=
ENST00000339797.5:c.1320C= ENSP00000343486.1:p.Ser440=
ENST00000351556.7:c.1320C= ENSP00000345878.3:p.Ser440=
ENST00000395559.6:c.1320C= ENSP00000378926.2:p.Ser440=
ENST00000395562.2:c.1428C= ENSP00000378929.2:p.Ser476=
ENST00000466590.6:c.*1405C= ENSP00000473443.1:n.*1405C=
NM_001142929.1:c.1320C= NP_001136401.1:p.Ser440=
NM_001142933.1:c.1428C= NP_001136405.1:p.Ser476=
NM_001142934.1:c.1320C= NP_001136406.1:p.Ser440=
NM_020549.4:c.1674C= NP_065574.3:p.Ser558=
NM_020984.3:c.1320C= NP_066264.3:p.Ser440=
NM_020985.3:c.1320C= NP_066265.3:p.Ser440=
NM_020986.3:c.1320C= NP_066266.3:p.Ser440=
NM_001142929.2:c.1320C= NP_001136401.2:p.Ser440=
NM_001142933.2:c.1428C= NP_001136405.2:p.Ser476=
NM_001142934.2:c.1320C= NP_001136406.2:p.Ser440=
NM_020549.5:c.1674C= MANE Select NP_065574.4:p.Ser558=
NM_020984.4:c.1320C= NP_066264.4:p.Ser440=
NM_020985.4:c.1320C= NP_066265.4:p.Ser440=
NM_020986.4:c.1320C= NP_066266.4:p.Ser440=