Canonical Allele Identifier: CA4202027

Gene: CHN2

Linked Data

• dbSNP Id: rs758187640
• ExAC: 7:29438015 A / G
• gnomAD v2: 7-29438015-A-G
• gnomAD v4: 7-29398399-A-G
• MyVariant Identifiers: chr7:g.29438015A>G (hg19) ; chr7:g.29398399A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398399A>G , CM000669.2:g.29398399A>G	GRCh38
NC_000007.13:g.29438015A>G , CM000669.1:g.29438015A>G	GRCh37
NC_000007.12:g.29404540A>G	NCBI36
NG_029365.2:g.256853A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409350.6:c.242A>G	ENSP00000386968.2:p.Gln81Arg
ENST00000439384.6:n.465A>G
ENST00000446446.6:c.203A>G	ENSP00000396867.2:p.Gln68Arg
ENST00000706158.1:c.*147A>G	ENSP00000516236.1:n.*147A>G
ENST00000706159.1:c.115A>G	ENSP00000516237.1:p.Arg39Gly
ENST00000706160.1:c.203A>G	ENSP00000516238.1:p.Gln68Arg
ENST00000706161.1:c.281A>G	ENSP00000516239.1:p.Gln94Arg
ENST00000706162.1:c.203A>G	ENSP00000516240.1:p.Gln68Arg
ENST00000706163.1:c.50-81880A>G	ENSP00000516241.1:n.50-81880A>G
ENST00000222792.11:c.203A>G MANE Select	ENSP00000222792.7:p.Gln68Arg
ENST00000644824.1:c.428A>G	ENSP00000495614.1:p.Gln143Arg
ENST00000222792.10:c.203A>G	ENSP00000222792.6:p.Gln68Arg
ENST00000409350.5:c.242A>G	ENSP00000386968.1:p.Gln81Arg
ENST00000409922.5:n.414A>G
ENST00000409964.6:n.402A>G
ENST00000412536.5:n.223A>G
ENST00000435288.6:c.168+4697A>G	ENSP00000400282.3:n.168+4697A>G
ENST00000439384.5:c.428A>G	ENSP00000409843.1:p.Gln143Arg
ENST00000474070.5:c.303A>G
ENST00000478128.6:n.297A>G
ENST00000482820.6:n.412A>G
ENST00000491856.1:n.1752A>G
ENST00000495789.6:c.203A>G	ENSP00000438587.2:p.Gln68Arg
ENST00000539389.5:c.203A>G	ENSP00000440526.2:p.Gln68Arg
ENST00000539406.5:c.203A>G	ENSP00000444063.2:p.Gln68Arg
NM_001293069.1:c.428A>G	NP_001279998.1:p.Gln143Arg
NM_001293070.1:c.242A>G	NP_001279999.1:p.Gln81Arg
NM_001293071.1:c.98A>G	NP_001280000.1:p.Gln33Arg
NM_001293072.1:c.158A>G	NP_001280001.1:p.Gln53Arg
NM_004067.3:c.203A>G	NP_004058.1:p.Gln68Arg
XM_011515105.1:c.506A>G	XP_011513407.1:p.Gln169Arg
XM_011515106.1:c.467A>G	XP_011513408.1:p.Gln156Arg
XM_011515107.1:c.281A>G	XP_011513409.1:p.Gln94Arg
XM_011515108.1:c.203A>G	XP_011513410.1:p.Gln68Arg
XM_011515109.1:c.164A>G	XP_011513411.1:p.Gln55Arg
XM_011515110.1:c.125A>G	XP_011513412.1:p.Gln42Arg
XM_011515111.1:c.98A>G	XP_011513413.1:p.Gln33Arg
XM_011515112.1:c.506A>G	XP_011513414.1:p.Gln169Arg
XM_011515105.2:c.506A>G	XP_011513407.1:p.Gln169Arg
XM_011515106.2:c.467A>G	XP_011513408.1:p.Gln156Arg
XM_011515107.2:c.281A>G	XP_011513409.1:p.Gln94Arg
XM_017011721.1:c.524A>G	XP_016867210.1:p.Gln175Arg
XM_017011722.1:c.299A>G	XP_016867211.1:p.Gln100Arg
NM_004067.4:c.203A>G MANE Select	NP_004058.1:p.Gln68Arg
NM_001293070.2:c.242A>G	NP_001279999.1:p.Gln81Arg
NM_001293071.2:c.98A>G	NP_001280000.1:p.Gln33Arg
NM_001293072.2:c.158A>G	NP_001280001.1:p.Gln53Arg
NM_001398427.1:c.-236A>G	NP_001385356.1:n.-236A>G