Canonical Allele Identifier: CA454421606

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438058T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398442T>A , CM000669.2:g.29398442T>A	GRCh38
NC_000007.13:g.29438058T>A , CM000669.1:g.29438058T>A	GRCh37
NC_000007.12:g.29404583T>A	NCBI36
NG_029365.2:g.256896T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.285T>A	ENSP00000386968.2:p.Leu95=
ENST00000439384.6:n.508T>A
ENST00000446446.6:c.246T>A	ENSP00000396867.2:p.Leu82=
ENST00000706158.1:c.*190T>A	ENSP00000516236.1:n.*190T>A
ENST00000706159.1:c.158T>A	ENSP00000516237.1:p.Leu53Ter
ENST00000706160.1:c.246T>A	ENSP00000516238.1:p.Leu82=
ENST00000706161.1:c.324T>A	ENSP00000516239.1:p.Leu108=
ENST00000706162.1:c.246T>A	ENSP00000516240.1:p.Leu82=
ENST00000706163.1:c.50-81837T>A	ENSP00000516241.1:n.50-81837T>A
ENST00000222792.11:c.246T>A MANE Select	ENSP00000222792.7:p.Leu82=
ENST00000644824.1:c.471T>A	ENSP00000495614.1:p.Leu157=
ENST00000222792.10:c.246T>A	ENSP00000222792.6:p.Leu82=
ENST00000409350.5:c.285T>A	ENSP00000386968.1:p.Leu95=
ENST00000409922.5:n.457T>A
ENST00000409964.6:n.445T>A
ENST00000412536.5:n.266T>A
ENST00000435288.6:c.168+4740T>A	ENSP00000400282.3:n.168+4740T>A
ENST00000439384.5:c.471T>A	ENSP00000409843.1:p.Leu157=
ENST00000474070.5:c.346T>A
ENST00000478128.6:n.340T>A
ENST00000482820.6:n.455T>A
ENST00000491856.1:n.1795T>A
ENST00000495789.6:c.246T>A	ENSP00000438587.2:p.Leu82=
ENST00000539389.5:c.246T>A	ENSP00000440526.2:p.Leu82=
ENST00000539406.5:c.246T>A	ENSP00000444063.2:p.Leu82=
NM_001293069.1:c.471T>A	NP_001279998.1:p.Leu157=
NM_001293070.1:c.285T>A	NP_001279999.1:p.Leu95=
NM_001293071.1:c.141T>A	NP_001280000.1:p.Leu47=
NM_001293072.1:c.201T>A	NP_001280001.1:p.Leu67=
NM_004067.3:c.246T>A	NP_004058.1:p.Leu82=
XM_011515105.1:c.549T>A	XP_011513407.1:p.Leu183=
XM_011515106.1:c.510T>A	XP_011513408.1:p.Leu170=
XM_011515107.1:c.324T>A	XP_011513409.1:p.Leu108=
XM_011515108.1:c.246T>A	XP_011513410.1:p.Leu82=
XM_011515109.1:c.207T>A	XP_011513411.1:p.Leu69=
XM_011515110.1:c.168T>A	XP_011513412.1:p.Leu56=
XM_011515111.1:c.141T>A	XP_011513413.1:p.Leu47=
XM_011515112.1:c.549T>A	XP_011513414.1:p.Leu183=
XM_011515105.2:c.549T>A	XP_011513407.1:p.Leu183=
XM_011515106.2:c.510T>A	XP_011513408.1:p.Leu170=
XM_011515107.2:c.324T>A	XP_011513409.1:p.Leu108=
XM_017011721.1:c.567T>A	XP_016867210.1:p.Leu189=
XM_017011722.1:c.342T>A	XP_016867211.1:p.Leu114=
NM_004067.4:c.246T>A MANE Select	NP_004058.1:p.Leu82=
NM_001293070.2:c.285T>A	NP_001279999.1:p.Leu95=
NM_001293071.2:c.141T>A	NP_001280000.1:p.Leu47=
NM_001293072.2:c.201T>A	NP_001280001.1:p.Leu67=
NM_001398427.1:c.-193T>A	NP_001385356.1:n.-193T>A