Canonical Allele Identifier: CA367241796

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438093T>G (hg19) ; chr7:g.29398477T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398477T>G , CM000669.2:g.29398477T>G	GRCh38
NC_000007.13:g.29438093T>G , CM000669.1:g.29438093T>G	GRCh37
NC_000007.12:g.29404618T>G	NCBI36
NG_029365.2:g.256931T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.320T>G	ENSP00000386968.2:p.Leu107Arg
ENST00000439384.6:n.543T>G
ENST00000446446.6:c.281T>G	ENSP00000396867.2:p.Leu94Arg
ENST00000706158.1:c.*225T>G	ENSP00000516236.1:n.*225T>G
ENST00000706159.1:c.193T>G	ENSP00000516237.1:p.Trp65Gly
ENST00000706160.1:c.281T>G	ENSP00000516238.1:p.Leu94Arg
ENST00000706161.1:c.359T>G	ENSP00000516239.1:p.Leu120Arg
ENST00000706162.1:c.281T>G	ENSP00000516240.1:p.Leu94Arg
ENST00000706163.1:c.50-81802T>G	ENSP00000516241.1:n.50-81802T>G
ENST00000222792.11:c.281T>G MANE Select	ENSP00000222792.7:p.Leu94Arg
ENST00000644824.1:c.506T>G	ENSP00000495614.1:p.Leu169Arg
ENST00000222792.10:c.281T>G	ENSP00000222792.6:p.Leu94Arg
ENST00000409350.5:c.320T>G	ENSP00000386968.1:p.Leu107Arg
ENST00000409922.5:n.492T>G
ENST00000409964.6:n.480T>G
ENST00000412536.5:n.301T>G
ENST00000435288.6:c.168+4775T>G	ENSP00000400282.3:n.168+4775T>G
ENST00000439384.5:c.506T>G	ENSP00000409843.1:p.Leu169Arg
ENST00000474070.5:c.381T>G
ENST00000478128.6:n.375T>G
ENST00000482820.6:n.490T>G
ENST00000491856.1:n.1830T>G
ENST00000495789.6:c.281T>G	ENSP00000438587.2:p.Leu94Arg
ENST00000539389.5:c.281T>G	ENSP00000440526.2:p.Leu94Arg
ENST00000539406.5:c.281T>G	ENSP00000444063.2:p.Leu94Arg
NM_001293069.1:c.506T>G	NP_001279998.1:p.Leu169Arg
NM_001293070.1:c.320T>G	NP_001279999.1:p.Leu107Arg
NM_001293071.1:c.176T>G	NP_001280000.1:p.Leu59Arg
NM_001293072.1:c.236T>G	NP_001280001.1:p.Leu79Arg
NM_004067.3:c.281T>G	NP_004058.1:p.Leu94Arg
XM_011515105.1:c.584T>G	XP_011513407.1:p.Leu195Arg
XM_011515106.1:c.545T>G	XP_011513408.1:p.Leu182Arg
XM_011515107.1:c.359T>G	XP_011513409.1:p.Leu120Arg
XM_011515108.1:c.281T>G	XP_011513410.1:p.Leu94Arg
XM_011515109.1:c.242T>G	XP_011513411.1:p.Leu81Arg
XM_011515110.1:c.203T>G	XP_011513412.1:p.Leu68Arg
XM_011515111.1:c.176T>G	XP_011513413.1:p.Leu59Arg
XM_011515112.1:c.584T>G	XP_011513414.1:p.Leu195Arg
XM_011515105.2:c.584T>G	XP_011513407.1:p.Leu195Arg
XM_011515106.2:c.545T>G	XP_011513408.1:p.Leu182Arg
XM_011515107.2:c.359T>G	XP_011513409.1:p.Leu120Arg
XM_017011721.1:c.602T>G	XP_016867210.1:p.Leu201Arg
XM_017011722.1:c.377T>G	XP_016867211.1:p.Leu126Arg
NM_004067.4:c.281T>G MANE Select	NP_004058.1:p.Leu94Arg
NM_001293070.2:c.320T>G	NP_001279999.1:p.Leu107Arg
NM_001293071.2:c.176T>G	NP_001280000.1:p.Leu59Arg
NM_001293072.2:c.236T>G	NP_001280001.1:p.Leu79Arg
NM_001398427.1:c.-158T>G	NP_001385356.1:n.-158T>G