Canonical Allele Identifier: CA1908834701

Gene: CHAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49655246G= , CM000672.2:g.49655246G=	GRCh38
NC_000010.10:g.50863292G= , CM000672.1:g.50863292G=	GRCh37
NC_000010.9:g.50533298G=	NCBI36
NG_011797.1:g.51152G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337653.7:c.1776+10G= MANE Select	ENSP00000337103.2:n.1776+10G=
ENST00000638282.1:c.*613+10G=	ENSP00000492646.1:n.*613+10G=
ENST00000638683.1:n.413+10G=
ENST00000640822.1:c.639+10G=	ENSP00000491328.1:n.639+10G=
ENST00000337653.6:c.1776+10G=	ENSP00000337103.2:n.1776+10G=
ENST00000339797.5:c.1422+10G=	ENSP00000343486.1:n.1422+10G=
ENST00000351556.7:c.1422+10G=	ENSP00000345878.3:n.1422+10G=
ENST00000395559.6:c.1422+10G=	ENSP00000378926.2:n.1422+10G=
ENST00000395562.2:c.1530+10G=	ENSP00000378929.2:n.1530+10G=
ENST00000466590.6:c.*1507+10G=	ENSP00000473443.1:n.*1507+10G=
NM_001142929.1:c.1422+10G=	NP_001136401.1:n.1422+10G=
NM_001142933.1:c.1530+10G=	NP_001136405.1:n.1530+10G=
NM_001142934.1:c.1422+10G=	NP_001136406.1:n.1422+10G=
NM_020549.4:c.1776+10G=	NP_065574.3:n.1776+10G=
NM_020984.3:c.1422+10G=	NP_066264.3:n.1422+10G=
NM_020985.3:c.1422+10G=	NP_066265.3:n.1422+10G=
NM_020986.3:c.1422+10G=	NP_066266.3:n.1422+10G=
NM_001142929.2:c.1422+10G=	NP_001136401.2:n.1422+10G=
NM_001142933.2:c.1530+10G=	NP_001136405.2:n.1530+10G=
NM_001142934.2:c.1422+10G=	NP_001136406.2:n.1422+10G=
NM_020549.5:c.1776+10G= MANE Select	NP_065574.4:n.1776+10G=
NM_020984.4:c.1422+10G=	NP_066264.4:n.1422+10G=
NM_020985.4:c.1422+10G=	NP_066265.4:n.1422+10G=
NM_020986.4:c.1422+10G=	NP_066266.4:n.1422+10G=