Canonical Allele Identifier: CA367241748

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438071C>G (hg19) ; chr7:g.29398455C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398455C>G , CM000669.2:g.29398455C>G	GRCh38
NC_000007.13:g.29438071C>G , CM000669.1:g.29438071C>G	GRCh37
NC_000007.12:g.29404596C>G	NCBI36
NG_029365.2:g.256909C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.298C>G	ENSP00000386968.2:p.Arg100Gly
ENST00000439384.6:n.521C>G
ENST00000446446.6:c.259C>G	ENSP00000396867.2:p.Arg87Gly
ENST00000706158.1:c.*203C>G	ENSP00000516236.1:n.*203C>G
ENST00000706159.1:c.171C>G	ENSP00000516237.1:p.Ser57Arg
ENST00000706160.1:c.259C>G	ENSP00000516238.1:p.Arg87Gly
ENST00000706161.1:c.337C>G	ENSP00000516239.1:p.Arg113Gly
ENST00000706162.1:c.259C>G	ENSP00000516240.1:p.Arg87Gly
ENST00000706163.1:c.50-81824C>G	ENSP00000516241.1:n.50-81824C>G
ENST00000222792.11:c.259C>G MANE Select	ENSP00000222792.7:p.Arg87Gly
ENST00000644824.1:c.484C>G	ENSP00000495614.1:p.Arg162Gly
ENST00000222792.10:c.259C>G	ENSP00000222792.6:p.Arg87Gly
ENST00000409350.5:c.298C>G	ENSP00000386968.1:p.Arg100Gly
ENST00000409922.5:n.470C>G
ENST00000409964.6:n.458C>G
ENST00000412536.5:n.279C>G
ENST00000435288.6:c.168+4753C>G	ENSP00000400282.3:n.168+4753C>G
ENST00000439384.5:c.484C>G	ENSP00000409843.1:p.Arg162Gly
ENST00000474070.5:c.359C>G
ENST00000478128.6:n.353C>G
ENST00000482820.6:n.468C>G
ENST00000491856.1:n.1808C>G
ENST00000495789.6:c.259C>G	ENSP00000438587.2:p.Arg87Gly
ENST00000539389.5:c.259C>G	ENSP00000440526.2:p.Arg87Gly
ENST00000539406.5:c.259C>G	ENSP00000444063.2:p.Arg87Gly
NM_001293069.1:c.484C>G	NP_001279998.1:p.Arg162Gly
NM_001293070.1:c.298C>G	NP_001279999.1:p.Arg100Gly
NM_001293071.1:c.154C>G	NP_001280000.1:p.Arg52Gly
NM_001293072.1:c.214C>G	NP_001280001.1:p.Arg72Gly
NM_004067.3:c.259C>G	NP_004058.1:p.Arg87Gly
XM_011515105.1:c.562C>G	XP_011513407.1:p.Arg188Gly
XM_011515106.1:c.523C>G	XP_011513408.1:p.Arg175Gly
XM_011515107.1:c.337C>G	XP_011513409.1:p.Arg113Gly
XM_011515108.1:c.259C>G	XP_011513410.1:p.Arg87Gly
XM_011515109.1:c.220C>G	XP_011513411.1:p.Arg74Gly
XM_011515110.1:c.181C>G	XP_011513412.1:p.Arg61Gly
XM_011515111.1:c.154C>G	XP_011513413.1:p.Arg52Gly
XM_011515112.1:c.562C>G	XP_011513414.1:p.Arg188Gly
XM_011515105.2:c.562C>G	XP_011513407.1:p.Arg188Gly
XM_011515106.2:c.523C>G	XP_011513408.1:p.Arg175Gly
XM_011515107.2:c.337C>G	XP_011513409.1:p.Arg113Gly
XM_017011721.1:c.580C>G	XP_016867210.1:p.Arg194Gly
XM_017011722.1:c.355C>G	XP_016867211.1:p.Arg119Gly
NM_004067.4:c.259C>G MANE Select	NP_004058.1:p.Arg87Gly
NM_001293070.2:c.298C>G	NP_001279999.1:p.Arg100Gly
NM_001293071.2:c.154C>G	NP_001280000.1:p.Arg52Gly
NM_001293072.2:c.214C>G	NP_001280001.1:p.Arg72Gly
NM_001398427.1:c.-180C>G	NP_001385356.1:n.-180C>G