Canonical Allele Identifier: CA367241689

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438045G>T (hg19) ; chr7:g.29398429G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398429G>T , CM000669.2:g.29398429G>T	GRCh38
NC_000007.13:g.29438045G>T , CM000669.1:g.29438045G>T	GRCh37
NC_000007.12:g.29404570G>T	NCBI36
NG_029365.2:g.256883G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.272G>T	ENSP00000386968.2:p.Gly91Val
ENST00000439384.6:n.495G>T
ENST00000446446.6:c.233G>T	ENSP00000396867.2:p.Gly78Val
ENST00000706158.1:c.*177G>T	ENSP00000516236.1:n.*177G>T
ENST00000706159.1:c.145G>T	ENSP00000516237.1:p.Val49Leu
ENST00000706160.1:c.233G>T	ENSP00000516238.1:p.Gly78Val
ENST00000706161.1:c.311G>T	ENSP00000516239.1:p.Gly104Val
ENST00000706162.1:c.233G>T	ENSP00000516240.1:p.Gly78Val
ENST00000706163.1:c.50-81850G>T	ENSP00000516241.1:n.50-81850G>T
ENST00000222792.11:c.233G>T MANE Select	ENSP00000222792.7:p.Gly78Val
ENST00000644824.1:c.458G>T	ENSP00000495614.1:p.Gly153Val
ENST00000222792.10:c.233G>T	ENSP00000222792.6:p.Gly78Val
ENST00000409350.5:c.272G>T	ENSP00000386968.1:p.Gly91Val
ENST00000409922.5:n.444G>T
ENST00000409964.6:n.432G>T
ENST00000412536.5:n.253G>T
ENST00000435288.6:c.168+4727G>T	ENSP00000400282.3:n.168+4727G>T
ENST00000439384.5:c.458G>T	ENSP00000409843.1:p.Gly153Val
ENST00000474070.5:c.333G>T
ENST00000478128.6:n.327G>T
ENST00000482820.6:n.442G>T
ENST00000491856.1:n.1782G>T
ENST00000495789.6:c.233G>T	ENSP00000438587.2:p.Gly78Val
ENST00000539389.5:c.233G>T	ENSP00000440526.2:p.Gly78Val
ENST00000539406.5:c.233G>T	ENSP00000444063.2:p.Gly78Val
NM_001293069.1:c.458G>T	NP_001279998.1:p.Gly153Val
NM_001293070.1:c.272G>T	NP_001279999.1:p.Gly91Val
NM_001293071.1:c.128G>T	NP_001280000.1:p.Gly43Val
NM_001293072.1:c.188G>T	NP_001280001.1:p.Gly63Val
NM_004067.3:c.233G>T	NP_004058.1:p.Gly78Val
XM_011515105.1:c.536G>T	XP_011513407.1:p.Gly179Val
XM_011515106.1:c.497G>T	XP_011513408.1:p.Gly166Val
XM_011515107.1:c.311G>T	XP_011513409.1:p.Gly104Val
XM_011515108.1:c.233G>T	XP_011513410.1:p.Gly78Val
XM_011515109.1:c.194G>T	XP_011513411.1:p.Gly65Val
XM_011515110.1:c.155G>T	XP_011513412.1:p.Gly52Val
XM_011515111.1:c.128G>T	XP_011513413.1:p.Gly43Val
XM_011515112.1:c.536G>T	XP_011513414.1:p.Gly179Val
XM_011515105.2:c.536G>T	XP_011513407.1:p.Gly179Val
XM_011515106.2:c.497G>T	XP_011513408.1:p.Gly166Val
XM_011515107.2:c.311G>T	XP_011513409.1:p.Gly104Val
XM_017011721.1:c.554G>T	XP_016867210.1:p.Gly185Val
XM_017011722.1:c.329G>T	XP_016867211.1:p.Gly110Val
NM_004067.4:c.233G>T MANE Select	NP_004058.1:p.Gly78Val
NM_001293070.2:c.272G>T	NP_001279999.1:p.Gly91Val
NM_001293071.2:c.128G>T	NP_001280000.1:p.Gly43Val
NM_001293072.2:c.188G>T	NP_001280001.1:p.Gly63Val
NM_001398427.1:c.-206G>T	NP_001385356.1:n.-206G>T