Canonical Allele Identifier: CA2839770207
Gene: CHAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49655340_49655341insGGGTTT , CM000672.2:g.49655340_49655341insGGGTTT GRCh38
NC_000010.10:g.50863386_50863387insGGGTTT , CM000672.1:g.50863386_50863387insGGGTTT GRCh37
NC_000010.9:g.50533392_50533393insGGGTTT NCBI36
NG_011797.1:g.51246_51247insGGGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000337653.7:c.1777-46_1777-45insGGGTTT MANE Select ENSP00000337103.2:n.1777-46_1777-45insGGGTTT
ENST00000638282.1:c.*614-46_*614-45insGGGTTT ENSP00000492646.1:n.*614-46_*614-45insGGGTTT
ENST00000638683.1:n.414-46_414-45insGGGTTT
ENST00000640822.1:c.640-46_640-45insGGGTTT ENSP00000491328.1:n.640-46_640-45insGGGTTT
ENST00000337653.6:c.1777-46_1777-45insGGGTTT ENSP00000337103.2:n.1777-46_1777-45insGGGTTT
ENST00000339797.5:c.1423-46_1423-45insGGGTTT ENSP00000343486.1:n.1423-46_1423-45insGGGTTT
ENST00000351556.7:c.1423-46_1423-45insGGGTTT ENSP00000345878.3:n.1423-46_1423-45insGGGTTT
ENST00000395559.6:c.1423-46_1423-45insGGGTTT ENSP00000378926.2:n.1423-46_1423-45insGGGTTT
ENST00000395562.2:c.1531-46_1531-45insGGGTTT ENSP00000378929.2:n.1531-46_1531-45insGGGTTT
ENST00000466590.6:c.*1508-46_*1508-45insGGGTTT ENSP00000473443.1:n.*1508-46_*1508-45insGGGTTT
NM_001142929.1:c.1423-46_1423-45insGGGTTT NP_001136401.1:n.1423-46_1423-45insGGGTTT
NM_001142933.1:c.1531-46_1531-45insGGGTTT NP_001136405.1:n.1531-46_1531-45insGGGTTT
NM_001142934.1:c.1423-46_1423-45insGGGTTT NP_001136406.1:n.1423-46_1423-45insGGGTTT
NM_020549.4:c.1777-46_1777-45insGGGTTT NP_065574.3:n.1777-46_1777-45insGGGTTT
NM_020984.3:c.1423-46_1423-45insGGGTTT NP_066264.3:n.1423-46_1423-45insGGGTTT
NM_020985.3:c.1423-46_1423-45insGGGTTT NP_066265.3:n.1423-46_1423-45insGGGTTT
NM_020986.3:c.1423-46_1423-45insGGGTTT NP_066266.3:n.1423-46_1423-45insGGGTTT
NM_001142929.2:c.1423-46_1423-45insGGGTTT NP_001136401.2:n.1423-46_1423-45insGGGTTT
NM_001142933.2:c.1531-46_1531-45insGGGTTT NP_001136405.2:n.1531-46_1531-45insGGGTTT
NM_001142934.2:c.1423-46_1423-45insGGGTTT NP_001136406.2:n.1423-46_1423-45insGGGTTT
NM_020549.5:c.1777-46_1777-45insGGGTTT MANE Select NP_065574.4:n.1777-46_1777-45insGGGTTT
NM_020984.4:c.1423-46_1423-45insGGGTTT NP_066264.4:n.1423-46_1423-45insGGGTTT
NM_020985.4:c.1423-46_1423-45insGGGTTT NP_066265.4:n.1423-46_1423-45insGGGTTT
NM_020986.4:c.1423-46_1423-45insGGGTTT NP_066266.4:n.1423-46_1423-45insGGGTTT