Canonical Allele Identifier: CA376747211

Gene: CHAT

Linked Data

• MyVariant Identifiers: chr10:g.50863167A>T (hg19) ; chr10:g.49655121A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49655121A>T , CM000672.2:g.49655121A>T	GRCh38
NC_000010.10:g.50863167A>T , CM000672.1:g.50863167A>T	GRCh37
NC_000010.9:g.50533173A>T	NCBI36
NG_011797.1:g.51027A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337653.7:c.1661A>T MANE Select	ENSP00000337103.2:p.Tyr554Phe
ENST00000638282.1:c.*498A>T	ENSP00000492646.1:n.*498A>T
ENST00000638683.1:n.298A>T
ENST00000640822.1:c.524A>T	ENSP00000491328.1:p.Tyr175Phe
ENST00000337653.6:c.1661A>T	ENSP00000337103.2:p.Tyr554Phe
ENST00000339797.5:c.1307A>T	ENSP00000343486.1:p.Tyr436Phe
ENST00000351556.7:c.1307A>T	ENSP00000345878.3:p.Tyr436Phe
ENST00000395559.6:c.1307A>T	ENSP00000378926.2:p.Tyr436Phe
ENST00000395562.2:c.1415A>T	ENSP00000378929.2:p.Tyr472Phe
ENST00000466590.6:c.*1392A>T	ENSP00000473443.1:n.*1392A>T
NM_001142929.1:c.1307A>T	NP_001136401.1:p.Tyr436Phe
NM_001142933.1:c.1415A>T	NP_001136405.1:p.Tyr472Phe
NM_001142934.1:c.1307A>T	NP_001136406.1:p.Tyr436Phe
NM_020549.4:c.1661A>T	NP_065574.3:p.Tyr554Phe
NM_020984.3:c.1307A>T	NP_066264.3:p.Tyr436Phe
NM_020985.3:c.1307A>T	NP_066265.3:p.Tyr436Phe
NM_020986.3:c.1307A>T	NP_066266.3:p.Tyr436Phe
NM_001142929.2:c.1307A>T	NP_001136401.2:p.Tyr436Phe
NM_001142933.2:c.1415A>T	NP_001136405.2:p.Tyr472Phe
NM_001142934.2:c.1307A>T	NP_001136406.2:p.Tyr436Phe
NM_020549.5:c.1661A>T MANE Select	NP_065574.4:p.Tyr554Phe
NM_020984.4:c.1307A>T	NP_066264.4:p.Tyr436Phe
NM_020985.4:c.1307A>T	NP_066265.4:p.Tyr436Phe
NM_020986.4:c.1307A>T	NP_066266.4:p.Tyr436Phe