Canonical Allele Identifier: CA367241651

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438026C>G (hg19) ; chr7:g.29398410C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398410C>G , CM000669.2:g.29398410C>G	GRCh38
NC_000007.13:g.29438026C>G , CM000669.1:g.29438026C>G	GRCh37
NC_000007.12:g.29404551C>G	NCBI36
NG_029365.2:g.256864C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.253C>G	ENSP00000386968.2:p.Leu85Val
ENST00000439384.6:n.476C>G
ENST00000446446.6:c.214C>G	ENSP00000396867.2:p.Leu72Val
ENST00000706158.1:c.*158C>G	ENSP00000516236.1:n.*158C>G
ENST00000706159.1:c.126C>G	ENSP00000516237.1:p.Ser42Arg
ENST00000706160.1:c.214C>G	ENSP00000516238.1:p.Leu72Val
ENST00000706161.1:c.292C>G	ENSP00000516239.1:p.Leu98Val
ENST00000706162.1:c.214C>G	ENSP00000516240.1:p.Leu72Val
ENST00000706163.1:c.50-81869C>G	ENSP00000516241.1:n.50-81869C>G
ENST00000222792.11:c.214C>G MANE Select	ENSP00000222792.7:p.Leu72Val
ENST00000644824.1:c.439C>G	ENSP00000495614.1:p.Leu147Val
ENST00000222792.10:c.214C>G	ENSP00000222792.6:p.Leu72Val
ENST00000409350.5:c.253C>G	ENSP00000386968.1:p.Leu85Val
ENST00000409922.5:n.425C>G
ENST00000409964.6:n.413C>G
ENST00000412536.5:n.234C>G
ENST00000435288.6:c.168+4708C>G	ENSP00000400282.3:n.168+4708C>G
ENST00000439384.5:c.439C>G	ENSP00000409843.1:p.Leu147Val
ENST00000474070.5:c.314C>G
ENST00000478128.6:n.308C>G
ENST00000482820.6:n.423C>G
ENST00000491856.1:n.1763C>G
ENST00000495789.6:c.214C>G	ENSP00000438587.2:p.Leu72Val
ENST00000539389.5:c.214C>G	ENSP00000440526.2:p.Leu72Val
ENST00000539406.5:c.214C>G	ENSP00000444063.2:p.Leu72Val
NM_001293069.1:c.439C>G	NP_001279998.1:p.Leu147Val
NM_001293070.1:c.253C>G	NP_001279999.1:p.Leu85Val
NM_001293071.1:c.109C>G	NP_001280000.1:p.Leu37Val
NM_001293072.1:c.169C>G	NP_001280001.1:p.Leu57Val
NM_004067.3:c.214C>G	NP_004058.1:p.Leu72Val
XM_011515105.1:c.517C>G	XP_011513407.1:p.Leu173Val
XM_011515106.1:c.478C>G	XP_011513408.1:p.Leu160Val
XM_011515107.1:c.292C>G	XP_011513409.1:p.Leu98Val
XM_011515108.1:c.214C>G	XP_011513410.1:p.Leu72Val
XM_011515109.1:c.175C>G	XP_011513411.1:p.Leu59Val
XM_011515110.1:c.136C>G	XP_011513412.1:p.Leu46Val
XM_011515111.1:c.109C>G	XP_011513413.1:p.Leu37Val
XM_011515112.1:c.517C>G	XP_011513414.1:p.Leu173Val
XM_011515105.2:c.517C>G	XP_011513407.1:p.Leu173Val
XM_011515106.2:c.478C>G	XP_011513408.1:p.Leu160Val
XM_011515107.2:c.292C>G	XP_011513409.1:p.Leu98Val
XM_017011721.1:c.535C>G	XP_016867210.1:p.Leu179Val
XM_017011722.1:c.310C>G	XP_016867211.1:p.Leu104Val
NM_004067.4:c.214C>G MANE Select	NP_004058.1:p.Leu72Val
NM_001293070.2:c.253C>G	NP_001279999.1:p.Leu85Val
NM_001293071.2:c.109C>G	NP_001280000.1:p.Leu37Val
NM_001293072.2:c.169C>G	NP_001280001.1:p.Leu57Val
NM_001398427.1:c.-225C>G	NP_001385356.1:n.-225C>G