Canonical Allele Identifier: CA7762522

Gene: CHSY1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101178325T>C , CM000677.2:g.101178325T>C	GRCh38
NC_000015.9:g.101718530T>C , CM000677.1:g.101718530T>C	GRCh37
NC_000015.8:g.99536053T>C	NCBI36
NG_031908.1:g.78608A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014918.5:c.1472A>G MANE Select	NP_055733.2:p.Gln491Arg
ENST00000254190.4:c.1472A>G MANE Select	ENSP00000254190.3:p.Gln491Arg
NM_014918.4:c.1472A>G	NP_055733.2:p.Gln491Arg
ENST00000254190.3:c.1472A>G	ENSP00000254190.3:p.Gln491Arg
ENST00000543813.1:n.725A>G
ENST00000543813.2:c.949A>G	ENSP00000496160.1:n.949A>G
XM_006720435.2:c.656A>G	XP_006720498.1:p.Gln219Arg
XM_006720435.3:c.656A>G	XP_006720498.1:p.Gln219Arg
XM_011521364.1:c.1556A>G	XP_011519666.1:p.Gln519Arg
XM_011521364.2:c.1556A>G	XP_011519666.1:p.Gln519Arg
XM_011521365.1:c.656A>G	XP_011519667.1:p.Gln219Arg
XM_017022011.1:c.656A>G	XP_016877500.1:p.Gln219Arg
XM_024449873.1:c.851A>G	XP_024305641.1:p.Gln284Arg