Canonical Allele Identifier: CA1908821576
Gene: CHAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49625545G= , CM000672.2:g.49625545G= GRCh38
NC_000010.10:g.50833591G= , CM000672.1:g.50833591G= GRCh37
NC_000010.9:g.50503597G= NCBI36
NG_011797.1:g.21451G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337653.7:c.825G= MANE Select ENSP00000337103.2:p.Gly275=
ENST00000337653.6:c.825G= ENSP00000337103.2:p.Gly275=
ENST00000339797.5:c.471G= ENSP00000343486.1:p.Gly157=
ENST00000351556.7:c.471G= ENSP00000345878.3:p.Gly157=
ENST00000395559.6:c.471G= ENSP00000378926.2:p.Gly157=
ENST00000395562.2:c.579G= ENSP00000378929.2:p.Gly193=
ENST00000466590.6:c.*556G= ENSP00000473443.1:n.*556G=
NM_001142929.1:c.471G= NP_001136401.1:p.Gly157=
NM_001142933.1:c.579G= NP_001136405.1:p.Gly193=
NM_001142934.1:c.471G= NP_001136406.1:p.Gly157=
NM_020549.4:c.825G= NP_065574.3:p.Gly275=
NM_020984.3:c.471G= NP_066264.3:p.Gly157=
NM_020985.3:c.471G= NP_066265.3:p.Gly157=
NM_020986.3:c.471G= NP_066266.3:p.Gly157=
NM_001142929.2:c.471G= NP_001136401.2:p.Gly157=
NM_001142933.2:c.579G= NP_001136405.2:p.Gly193=
NM_001142934.2:c.471G= NP_001136406.2:p.Gly157=
NM_020549.5:c.825G= MANE Select NP_065574.4:p.Gly275=
NM_020984.4:c.471G= NP_066264.4:p.Gly157=
NM_020985.4:c.471G= NP_066265.4:p.Gly157=
NM_020986.4:c.471G= NP_066266.4:p.Gly157=