Canonical Allele Identifier: CA2609117916

Gene: CHAT

Linked Data

• gnomAD v4: 10-49654949-A-AGAATTCTAGAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49654957_49654958insGAGGGAATTCTA , CM000672.2:g.49654957_49654958insGAGGGAATTCTA	GRCh38
NC_000010.10:g.50863003_50863004insGAGGGAATTCTA , CM000672.1:g.50863003_50863004insGAGGGAATTCTA	GRCh37
NC_000010.9:g.50533009_50533010insGAGGGAATTCTA	NCBI36
NG_011797.1:g.50863_50864insGAGGGAATTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337653.7:c.1635-138_1635-137insGAGGGAATTCTA MANE Select	ENSP00000337103.2:n.1635-138_1635-137insGAGGGAATTCTA
ENST00000638282.1:c.*472-138_*472-137insGAGGGAATTCTA	ENSP00000492646.1:n.*472-138_*472-137insGAGGGAATTCTA
ENST00000638683.1:n.272-138_272-137insGAGGGAATTCTA
ENST00000640822.1:c.498-138_498-137insGAGGGAATTCTA	ENSP00000491328.1:n.498-138_498-137insGAGGGAATTCTA
ENST00000337653.6:c.1635-138_1635-137insGAGGGAATTCTA	ENSP00000337103.2:n.1635-138_1635-137insGAGGGAATTCTA
ENST00000339797.5:c.1281-138_1281-137insGAGGGAATTCTA	ENSP00000343486.1:n.1281-138_1281-137insGAGGGAATTCTA
ENST00000351556.7:c.1281-138_1281-137insGAGGGAATTCTA	ENSP00000345878.3:n.1281-138_1281-137insGAGGGAATTCTA
ENST00000395559.6:c.1281-138_1281-137insGAGGGAATTCTA	ENSP00000378926.2:n.1281-138_1281-137insGAGGGAATTCTA
ENST00000395562.2:c.1389-138_1389-137insGAGGGAATTCTA	ENSP00000378929.2:n.1389-138_1389-137insGAGGGAATTCTA
ENST00000466590.6:c.*1366-138_*1366-137insGAGGGAATTCTA	ENSP00000473443.1:n.*1366-138_*1366-137insGAGGGAATTCTA
NM_001142929.1:c.1281-138_1281-137insGAGGGAATTCTA	NP_001136401.1:n.1281-138_1281-137insGAGGGAATTCTA
NM_001142933.1:c.1389-138_1389-137insGAGGGAATTCTA	NP_001136405.1:n.1389-138_1389-137insGAGGGAATTCTA
NM_001142934.1:c.1281-138_1281-137insGAGGGAATTCTA	NP_001136406.1:n.1281-138_1281-137insGAGGGAATTCTA
NM_020549.4:c.1635-138_1635-137insGAGGGAATTCTA	NP_065574.3:n.1635-138_1635-137insGAGGGAATTCTA
NM_020984.3:c.1281-138_1281-137insGAGGGAATTCTA	NP_066264.3:n.1281-138_1281-137insGAGGGAATTCTA
NM_020985.3:c.1281-138_1281-137insGAGGGAATTCTA	NP_066265.3:n.1281-138_1281-137insGAGGGAATTCTA
NM_020986.3:c.1281-138_1281-137insGAGGGAATTCTA	NP_066266.3:n.1281-138_1281-137insGAGGGAATTCTA
NM_001142929.2:c.1281-138_1281-137insGAGGGAATTCTA	NP_001136401.2:n.1281-138_1281-137insGAGGGAATTCTA
NM_001142933.2:c.1389-138_1389-137insGAGGGAATTCTA	NP_001136405.2:n.1389-138_1389-137insGAGGGAATTCTA
NM_001142934.2:c.1281-138_1281-137insGAGGGAATTCTA	NP_001136406.2:n.1281-138_1281-137insGAGGGAATTCTA
NM_020549.5:c.1635-138_1635-137insGAGGGAATTCTA MANE Select	NP_065574.4:n.1635-138_1635-137insGAGGGAATTCTA
NM_020984.4:c.1281-138_1281-137insGAGGGAATTCTA	NP_066264.4:n.1281-138_1281-137insGAGGGAATTCTA
NM_020985.4:c.1281-138_1281-137insGAGGGAATTCTA	NP_066265.4:n.1281-138_1281-137insGAGGGAATTCTA
NM_020986.4:c.1281-138_1281-137insGAGGGAATTCTA	NP_066266.4:n.1281-138_1281-137insGAGGGAATTCTA