Canonical Allele Identifier: CA454421617

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438073G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398457G>T , CM000669.2:g.29398457G>T	GRCh38
NC_000007.13:g.29438073G>T , CM000669.1:g.29438073G>T	GRCh37
NC_000007.12:g.29404598G>T	NCBI36
NG_029365.2:g.256911G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.300G>T	ENSP00000386968.2:p.Arg100=
ENST00000439384.6:n.523G>T
ENST00000446446.6:c.261G>T	ENSP00000396867.2:p.Arg87=
ENST00000706158.1:c.*205G>T	ENSP00000516236.1:n.*205G>T
ENST00000706159.1:c.173G>T	ENSP00000516237.1:p.Gly58Val
ENST00000706160.1:c.261G>T	ENSP00000516238.1:p.Arg87=
ENST00000706161.1:c.339G>T	ENSP00000516239.1:p.Arg113=
ENST00000706162.1:c.261G>T	ENSP00000516240.1:p.Arg87=
ENST00000706163.1:c.50-81822G>T	ENSP00000516241.1:n.50-81822G>T
ENST00000222792.11:c.261G>T MANE Select	ENSP00000222792.7:p.Arg87=
ENST00000644824.1:c.486G>T	ENSP00000495614.1:p.Arg162=
ENST00000222792.10:c.261G>T	ENSP00000222792.6:p.Arg87=
ENST00000409350.5:c.300G>T	ENSP00000386968.1:p.Arg100=
ENST00000409922.5:n.472G>T
ENST00000409964.6:n.460G>T
ENST00000412536.5:n.281G>T
ENST00000435288.6:c.168+4755G>T	ENSP00000400282.3:n.168+4755G>T
ENST00000439384.5:c.486G>T	ENSP00000409843.1:p.Arg162=
ENST00000474070.5:c.361G>T
ENST00000478128.6:n.355G>T
ENST00000482820.6:n.470G>T
ENST00000491856.1:n.1810G>T
ENST00000495789.6:c.261G>T	ENSP00000438587.2:p.Arg87=
ENST00000539389.5:c.261G>T	ENSP00000440526.2:p.Arg87=
ENST00000539406.5:c.261G>T	ENSP00000444063.2:p.Arg87=
NM_001293069.1:c.486G>T	NP_001279998.1:p.Arg162=
NM_001293070.1:c.300G>T	NP_001279999.1:p.Arg100=
NM_001293071.1:c.156G>T	NP_001280000.1:p.Arg52=
NM_001293072.1:c.216G>T	NP_001280001.1:p.Arg72=
NM_004067.3:c.261G>T	NP_004058.1:p.Arg87=
XM_011515105.1:c.564G>T	XP_011513407.1:p.Arg188=
XM_011515106.1:c.525G>T	XP_011513408.1:p.Arg175=
XM_011515107.1:c.339G>T	XP_011513409.1:p.Arg113=
XM_011515108.1:c.261G>T	XP_011513410.1:p.Arg87=
XM_011515109.1:c.222G>T	XP_011513411.1:p.Arg74=
XM_011515110.1:c.183G>T	XP_011513412.1:p.Arg61=
XM_011515111.1:c.156G>T	XP_011513413.1:p.Arg52=
XM_011515112.1:c.564G>T	XP_011513414.1:p.Arg188=
XM_011515105.2:c.564G>T	XP_011513407.1:p.Arg188=
XM_011515106.2:c.525G>T	XP_011513408.1:p.Arg175=
XM_011515107.2:c.339G>T	XP_011513409.1:p.Arg113=
XM_017011721.1:c.582G>T	XP_016867210.1:p.Arg194=
XM_017011722.1:c.357G>T	XP_016867211.1:p.Arg119=
NM_004067.4:c.261G>T MANE Select	NP_004058.1:p.Arg87=
NM_001293070.2:c.300G>T	NP_001279999.1:p.Arg100=
NM_001293071.2:c.156G>T	NP_001280000.1:p.Arg52=
NM_001293072.2:c.216G>T	NP_001280001.1:p.Arg72=
NM_001398427.1:c.-178G>T	NP_001385356.1:n.-178G>T