Canonical Allele Identifier: CA1630848235

Gene: CHAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49616071G= , CM000672.2:g.49616071G=	GRCh38
NC_000010.10:g.50824117G= , CM000672.1:g.50824117G=	GRCh37
NC_000010.9:g.50494123G=	NCBI36
NG_011797.1:g.11977G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020549.5:c.287-431G= MANE Select	NP_065574.4:n.287-431G=
ENST00000337653.7:c.287-431G= MANE Select	ENSP00000337103.2:n.287-431G=
NM_001142929.1:c.-68-431G=	NP_001136401.1:n.-68-431G=
NM_001142929.2:c.-68-431G=	NP_001136401.2:n.-68-431G=
NM_001142933.1:c.19G=	NP_001136405.1:p.Asp7=
NM_001142933.2:c.19G=	NP_001136405.2:p.Asp7=
NM_001142934.1:c.-90G=	NP_001136406.1:n.-90G=
NM_001142934.2:c.-90G=	NP_001136406.2:n.-90G=
NM_020549.4:c.287-431G=	NP_065574.3:n.287-431G=
NM_020984.3:c.-68-431G=	NP_066264.3:n.-68-431G=
NM_020984.4:c.-68-431G=	NP_066264.4:n.-68-431G=
NM_020985.3:c.-68-431G=	NP_066265.3:n.-68-431G=
NM_020985.4:c.-68-431G=	NP_066265.4:n.-68-431G=
NM_020986.3:c.-68-431G=	NP_066266.3:n.-68-431G=
NM_020986.4:c.-68-431G=	NP_066266.4:n.-68-431G=
ENST00000337653.6:c.287-431G=	ENSP00000337103.2:n.287-431G=
ENST00000339797.5:c.-68-431G=	ENSP00000343486.1:n.-68-431G=
ENST00000351556.7:c.-68-431G=	ENSP00000345878.3:n.-68-431G=
ENST00000395559.6:c.-68-431G=	ENSP00000378926.2:n.-68-431G=
ENST00000395562.2:c.19G=	ENSP00000378929.2:p.Asp7=
ENST00000460699.5:n.268-431G=
ENST00000466590.6:c.335G=	ENSP00000473443.1:p.Arg112=
ENST00000481336.5:n.85-431G=
ENST00000490270.1:n.315G=