Canonical Allele Identifier: CA367241714

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438057T>G (hg19) ; chr7:g.29398441T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398441T>G , CM000669.2:g.29398441T>G	GRCh38
NC_000007.13:g.29438057T>G , CM000669.1:g.29438057T>G	GRCh37
NC_000007.12:g.29404582T>G	NCBI36
NG_029365.2:g.256895T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.284T>G	ENSP00000386968.2:p.Leu95Arg
ENST00000439384.6:n.507T>G
ENST00000446446.6:c.245T>G	ENSP00000396867.2:p.Leu82Arg
ENST00000706158.1:c.*189T>G	ENSP00000516236.1:n.*189T>G
ENST00000706159.1:c.157T>G	ENSP00000516237.1:p.Leu53Val
ENST00000706160.1:c.245T>G	ENSP00000516238.1:p.Leu82Arg
ENST00000706161.1:c.323T>G	ENSP00000516239.1:p.Leu108Arg
ENST00000706162.1:c.245T>G	ENSP00000516240.1:p.Leu82Arg
ENST00000706163.1:c.50-81838T>G	ENSP00000516241.1:n.50-81838T>G
ENST00000222792.11:c.245T>G MANE Select	ENSP00000222792.7:p.Leu82Arg
ENST00000644824.1:c.470T>G	ENSP00000495614.1:p.Leu157Arg
ENST00000222792.10:c.245T>G	ENSP00000222792.6:p.Leu82Arg
ENST00000409350.5:c.284T>G	ENSP00000386968.1:p.Leu95Arg
ENST00000409922.5:n.456T>G
ENST00000409964.6:n.444T>G
ENST00000412536.5:n.265T>G
ENST00000435288.6:c.168+4739T>G	ENSP00000400282.3:n.168+4739T>G
ENST00000439384.5:c.470T>G	ENSP00000409843.1:p.Leu157Arg
ENST00000474070.5:c.345T>G
ENST00000478128.6:n.339T>G
ENST00000482820.6:n.454T>G
ENST00000491856.1:n.1794T>G
ENST00000495789.6:c.245T>G	ENSP00000438587.2:p.Leu82Arg
ENST00000539389.5:c.245T>G	ENSP00000440526.2:p.Leu82Arg
ENST00000539406.5:c.245T>G	ENSP00000444063.2:p.Leu82Arg
NM_001293069.1:c.470T>G	NP_001279998.1:p.Leu157Arg
NM_001293070.1:c.284T>G	NP_001279999.1:p.Leu95Arg
NM_001293071.1:c.140T>G	NP_001280000.1:p.Leu47Arg
NM_001293072.1:c.200T>G	NP_001280001.1:p.Leu67Arg
NM_004067.3:c.245T>G	NP_004058.1:p.Leu82Arg
XM_011515105.1:c.548T>G	XP_011513407.1:p.Leu183Arg
XM_011515106.1:c.509T>G	XP_011513408.1:p.Leu170Arg
XM_011515107.1:c.323T>G	XP_011513409.1:p.Leu108Arg
XM_011515108.1:c.245T>G	XP_011513410.1:p.Leu82Arg
XM_011515109.1:c.206T>G	XP_011513411.1:p.Leu69Arg
XM_011515110.1:c.167T>G	XP_011513412.1:p.Leu56Arg
XM_011515111.1:c.140T>G	XP_011513413.1:p.Leu47Arg
XM_011515112.1:c.548T>G	XP_011513414.1:p.Leu183Arg
XM_011515105.2:c.548T>G	XP_011513407.1:p.Leu183Arg
XM_011515106.2:c.509T>G	XP_011513408.1:p.Leu170Arg
XM_011515107.2:c.323T>G	XP_011513409.1:p.Leu108Arg
XM_017011721.1:c.566T>G	XP_016867210.1:p.Leu189Arg
XM_017011722.1:c.341T>G	XP_016867211.1:p.Leu114Arg
NM_004067.4:c.245T>G MANE Select	NP_004058.1:p.Leu82Arg
NM_001293070.2:c.284T>G	NP_001279999.1:p.Leu95Arg
NM_001293071.2:c.140T>G	NP_001280000.1:p.Leu47Arg
NM_001293072.2:c.200T>G	NP_001280001.1:p.Leu67Arg
NM_001398427.1:c.-194T>G	NP_001385356.1:n.-194T>G