Canonical Allele Identifier: CA376747447
Gene: CHAT HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000337653.7:c.1686C>A MANE Select ENSP00000337103.2:p.Phe562Leu
ENST00000638282.1:c.*523C>A ENSP00000492646.1:n.*523C>A
ENST00000638683.1:n.323C>A
ENST00000640822.1:c.549C>A ENSP00000491328.1:p.Phe183Leu
ENST00000337653.6:c.1686C>A ENSP00000337103.2:p.Phe562Leu
ENST00000339797.5:c.1332C>A ENSP00000343486.1:p.Phe444Leu
ENST00000351556.7:c.1332C>A ENSP00000345878.3:p.Phe444Leu
ENST00000395559.6:c.1332C>A ENSP00000378926.2:p.Phe444Leu
ENST00000395562.2:c.1440C>A ENSP00000378929.2:p.Phe480Leu
ENST00000466590.6:c.*1417C>A ENSP00000473443.1:n.*1417C>A
NM_001142929.1:c.1332C>A NP_001136401.1:p.Phe444Leu
NM_001142933.1:c.1440C>A NP_001136405.1:p.Phe480Leu
NM_001142934.1:c.1332C>A NP_001136406.1:p.Phe444Leu
NM_020549.4:c.1686C>A NP_065574.3:p.Phe562Leu
NM_020984.3:c.1332C>A NP_066264.3:p.Phe444Leu
NM_020985.3:c.1332C>A NP_066265.3:p.Phe444Leu
NM_020986.3:c.1332C>A NP_066266.3:p.Phe444Leu
NM_001142929.2:c.1332C>A NP_001136401.2:p.Phe444Leu
NM_001142933.2:c.1440C>A NP_001136405.2:p.Phe480Leu
NM_001142934.2:c.1332C>A NP_001136406.2:p.Phe444Leu
NM_020549.5:c.1686C>A MANE Select NP_065574.4:p.Phe562Leu
NM_020984.4:c.1332C>A NP_066264.4:p.Phe444Leu
NM_020985.4:c.1332C>A NP_066265.4:p.Phe444Leu
NM_020986.4:c.1332C>A NP_066266.4:p.Phe444Leu