Canonical Allele Identifier: CA13154240

Gene: CHAT

Linked Data

• ClinVar Variation Id: 678354
• ClinVar RCV Id: RCV000837934 ; RCV001578878
• dbSNP Id: rs12264845
• gnomAD v2: 10-50863083-A-C
• gnomAD v3: 10-49655037-A-C
• gnomAD v4: 10-49655037-A-C
• MyVariant Identifiers: chr10:g.50863083A>C (hg19) ; chr10:g.49655037A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49655037A>C , CM000672.2:g.49655037A>C	GRCh38
NC_000010.10:g.50863083A>C , CM000672.1:g.50863083A>C	GRCh37
NC_000010.9:g.50533089A>C	NCBI36
NG_011797.1:g.50943A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000337653.7:c.1635-58A>C MANE Select	ENSP00000337103.2:n.1635-58A>C
ENST00000638282.1:c.*472-58A>C	ENSP00000492646.1:n.*472-58A>C
ENST00000638683.1:n.272-58A>C
ENST00000640822.1:c.498-58A>C	ENSP00000491328.1:n.498-58A>C
ENST00000337653.6:c.1635-58A>C	ENSP00000337103.2:n.1635-58A>C
ENST00000339797.5:c.1281-58A>C	ENSP00000343486.1:n.1281-58A>C
ENST00000351556.7:c.1281-58A>C	ENSP00000345878.3:n.1281-58A>C
ENST00000395559.6:c.1281-58A>C	ENSP00000378926.2:n.1281-58A>C
ENST00000395562.2:c.1389-58A>C	ENSP00000378929.2:n.1389-58A>C
ENST00000466590.6:c.*1366-58A>C	ENSP00000473443.1:n.*1366-58A>C
NM_001142929.1:c.1281-58A>C	NP_001136401.1:n.1281-58A>C
NM_001142933.1:c.1389-58A>C	NP_001136405.1:n.1389-58A>C
NM_001142934.1:c.1281-58A>C	NP_001136406.1:n.1281-58A>C
NM_020549.4:c.1635-58A>C	NP_065574.3:n.1635-58A>C
NM_020984.3:c.1281-58A>C	NP_066264.3:n.1281-58A>C
NM_020985.3:c.1281-58A>C	NP_066265.3:n.1281-58A>C
NM_020986.3:c.1281-58A>C	NP_066266.3:n.1281-58A>C
NM_001142929.2:c.1281-58A>C	NP_001136401.2:n.1281-58A>C
NM_001142933.2:c.1389-58A>C	NP_001136405.2:n.1389-58A>C
NM_001142934.2:c.1281-58A>C	NP_001136406.2:n.1281-58A>C
NM_020549.5:c.1635-58A>C MANE Select	NP_065574.4:n.1635-58A>C
NM_020984.4:c.1281-58A>C	NP_066264.4:n.1281-58A>C
NM_020985.4:c.1281-58A>C	NP_066265.4:n.1281-58A>C
NM_020986.4:c.1281-58A>C	NP_066266.4:n.1281-58A>C