Canonical Allele Identifier: CA469605670

Gene: CHAT

Linked Data

• MyVariant Identifiers: chr10:g.50863192C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49655146C>T , CM000672.2:g.49655146C>T	GRCh38
NC_000010.10:g.50863192C>T , CM000672.1:g.50863192C>T	GRCh37
NC_000010.9:g.50533198C>T	NCBI36
NG_011797.1:g.51052C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000337653.7:c.1686C>T MANE Select	ENSP00000337103.2:p.Phe562=
ENST00000638282.1:c.*523C>T	ENSP00000492646.1:n.*523C>T
ENST00000638683.1:n.323C>T
ENST00000640822.1:c.549C>T	ENSP00000491328.1:p.Phe183=
ENST00000337653.6:c.1686C>T	ENSP00000337103.2:p.Phe562=
ENST00000339797.5:c.1332C>T	ENSP00000343486.1:p.Phe444=
ENST00000351556.7:c.1332C>T	ENSP00000345878.3:p.Phe444=
ENST00000395559.6:c.1332C>T	ENSP00000378926.2:p.Phe444=
ENST00000395562.2:c.1440C>T	ENSP00000378929.2:p.Phe480=
ENST00000466590.6:c.*1417C>T	ENSP00000473443.1:n.*1417C>T
NM_001142929.1:c.1332C>T	NP_001136401.1:p.Phe444=
NM_001142933.1:c.1440C>T	NP_001136405.1:p.Phe480=
NM_001142934.1:c.1332C>T	NP_001136406.1:p.Phe444=
NM_020549.4:c.1686C>T	NP_065574.3:p.Phe562=
NM_020984.3:c.1332C>T	NP_066264.3:p.Phe444=
NM_020985.3:c.1332C>T	NP_066265.3:p.Phe444=
NM_020986.3:c.1332C>T	NP_066266.3:p.Phe444=
NM_001142929.2:c.1332C>T	NP_001136401.2:p.Phe444=
NM_001142933.2:c.1440C>T	NP_001136405.2:p.Phe480=
NM_001142934.2:c.1332C>T	NP_001136406.2:p.Phe444=
NM_020549.5:c.1686C>T MANE Select	NP_065574.4:p.Phe562=
NM_020984.4:c.1332C>T	NP_066264.4:p.Phe444=
NM_020985.4:c.1332C>T	NP_066265.4:p.Phe444=
NM_020986.4:c.1332C>T	NP_066266.4:p.Phe444=